A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025979



Internal ID19115196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:24554120..24684865hg38UCSC Ensembl
Innerchr9:24554118..24684863hg19UCSC Ensembl
Innerchr9:24544118..24674863hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg38130746
hg19130746
hg18130746
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7481n100
Supporting Variantsnssv3690845
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)nsv1025979
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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