A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022474



Internal ID19111692
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:7735724..7770825hg38UCSC Ensembl
Innerchr9:7735724..7770825hg19UCSC Ensembl
Innerchr9:7725724..7760825hg18UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg3835102
hg1935102
hg1835102
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7393n100
Supporting Variantsnssv3689113
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)nsv1022474
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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