A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3730849



Internal ID19029130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:57310682..57467007hg38UCSC Ensembl
Innerchr2:57537817..57694142hg19UCSC Ensembl
Innerchr2:57391321..57547646hg18UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38156326
hg19156326
hg18156326
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1000899
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)nssv3730849
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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