A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003668



Internal ID19092886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:59296507..59365009hg38UCSC Ensembl
Innerchr2:59523642..59592144hg19UCSC Ensembl
Innerchr2:59377146..59445648hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg3868503
hg1968503
hg1868503
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3730850
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1003668
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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