A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999736



Internal ID19159272
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 StatusM
Merged Variants
Supporting Variantsnssv3729164
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)nsv999736
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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