A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5165



Internal ID9626824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:77390303..77467084hg38UCSC Ensembl
Innerchr6:78100020..78176801hg19UCSC Ensembl
Innerchr6:78156739..78233520hg18UCSC Ensembl
Innerchr6:78156739..78233520hg17UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3876782
hg1976782
hg1876782
hg1776782
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2758062
Supporting Variants
SamplesNA18564
Known GenesHTR1B
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)essv5165
Frequency
Sample Size270
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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