A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034657



Internal ID19123878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:16963865..16992327hg38UCSC Ensembl
Innerchr9:16963863..16992325hg19UCSC Ensembl
Innerchr9:16953863..16982325hg18UCSC Ensembl
Cytoband9p22.2
Allele length
AssemblyAllele length
hg3828463
hg1928463
hg1828463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690642
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)nsv1034657
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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