A curated catalogue of human genomic structural variation




Variant Details

Variant: essv16537



Internal ID9978145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:56730870..56930193hg38UCSC Ensembl
Innerchr10:58490630..58689953hg19UCSC Ensembl
Innerchr10:58160636..58359959hg18UCSC Ensembl
Innerchr10:58160636..58359959hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38199324
hg19199324
hg18199324
hg17199324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758223
Supporting Variants
SamplesNA19210
Known Genes
MethodBAC aCGH
AnalysisArray images were acquired using an Agilent laser scanner (Agilent Technologies, UK). Fluorescence intensities and log2 ratio values were extracted using Bluefuse software (Bluegnome Ltd).
PlatformAgilent
Comments
ReferenceRedon_et_al_2006
Pubmed ID17122850
Accession Number(s)essv16537
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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