A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3730850



Internal ID19029131
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 StatusS
Merged Variantsnsv1003668
Supporting Variants
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)nssv3730850
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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