A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011732



Internal ID19100950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:21600126..21634335hg38UCSC Ensembl
Innerchr2:21822998..21857207hg19UCSC Ensembl
Innerchr2:21676503..21710712hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3834210
hg1934210
hg1834210
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3740n100
Supporting Variantsnssv3579009, nssv3579008
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)nsv1011732
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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