A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012535



Internal ID18755068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:201662343..201700567hg38UCSC Ensembl
Innerchr1:201631471..201669695hg19UCSC Ensembl
Innerchr1:199898094..199936318hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3838225
hg1938225
hg1838225
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3496418
Samples
Known GenesIPO9-AS1, NAV1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012535
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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