A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038241



Internal ID19127460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:102181393..102283874hg38UCSC Ensembl
Innerchr9:104943675..105046156hg19UCSC Ensembl
Innerchr9:103983496..104085977hg18UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38102482
hg19102482
hg18102482
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697586
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)nsv1038241
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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