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Landmark or Region: Examples: chr7:71890181..72690180, CFTR, AC108171.3, nsv529033.
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Overview

Chromosome (overview)

Details

DGV Version 1 Structural Variants (Blue:Gain;Re...

Cytogenetic Bands

DGV Structural Variants (Blue:Gain;Red:Loss;Bro...

RefSeq Genes

UCSC segmental duplications

Disease Genes (OMIM)

DECIPHER Genomic Disorders

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Clones on WGTP Array [?]	Clones on SMRT BAC Array [?]	NimbleGen 385K Whole Genome Array [?]
Agilent 244k [?]	Cytochip V3.0 [?]

ISCA Curated clinically relevant regions [?]	Disease Genes (OMIM) [?]	DECIPHER: Chromosomal Imbalance and Phenotype in Humans (Blue:Gain;Red:Loss;Brown:Complex;Black:NA) [?]
ISCA Clinical cytogenetic testing (Blue:Gain;Red:Loss;Brown:Complex;Black:NA) [?]	DECIPHER Genomic Disorders [?]

Personal Genome Variants (Blue:Gain;Red:Loss;Brown:Complex;Purple:Inversion;Black:Unknown) [?]	SNPs [?]	RepeatMasker [?]
dbRIP [?]	Recombination hotspots [?]

DGV Structural Variants (Blue:Gain;Red:Loss;Brown:Complex;Purple:Inversion;Black:Unknown) [?]	DGV Version 1 Structural Variants (Blue:Gain;Red:Loss;Brown:Complex;Purple:Inversion;Black:Unknown) [?]
Supporting Variants (Blue:Gain;Red:Loss;Brown:Complex;Purple:Inverison;Black:Unknown) [?]	Unannotated Studies (Blue:Gain;Red:Loss;Brown:Complex;Purple:Inversion;Black:Unknown) [?]

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Show tooltips		Region Size (bp)

Genomic Variants in Human Genome (Build 36: Mar. 2006, hg18): 114.9 kbp from chr8:7,005..121,941