A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3732021



Internal ID19030302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:82751075..83100994hg38UCSC Ensembl
Innerchr2:82978199..83328118hg19UCSC Ensembl
Innerchr2:82831710..83181629hg18UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg38349920
hg19349920
hg18349920
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1014578
Supporting Variants
Samples
Known GenesLOC1720
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3732021
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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