A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034795



Internal ID19124016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:15565672..15595593hg38UCSC Ensembl
Innerchr9:15565670..15595591hg19UCSC Ensembl
Innerchr9:15555670..15585591hg18UCSC Ensembl
Cytoband9p22.3
Allele length
AssemblyAllele length
hg3829922
hg1929922
hg1829922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690627
Samples
Known GenesCCDC171
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034795
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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