A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3729164



Internal ID19027445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:98090206..98194612hg38UCSC Ensembl
Innerchr2:98706669..98811075hg19UCSC Ensembl
Innerchr2:98073101..98177507hg18UCSC Ensembl
Cytoband2q11.2
Allele length
AssemblyAllele length
hg38104407
hg19104407
hg18104407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv999736
Supporting Variants
Samples
Known GenesVWA3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3729164
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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