A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729325



Internal ID19027606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:194445496..194763432hg38UCSC Ensembl
Innerchr2:195310220..195628156hg19UCSC Ensembl
Innerchr2:195018465..195336401hg18UCSC Ensembl
Cytoband2q32.3
Allele length
AssemblyAllele length
hg38317937
hg19317937
hg18317937
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1008159
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)nssv3729325
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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