A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055156



Internal ID18797687
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:69243554..69276170hg38UCSC Ensembl
Innerchr17:67239695..67272311hg19UCSC Ensembl
Innerchr17:64751290..64783906hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3832617
hg1932617
hg1832617
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3567760
Samples
Known GenesABCA10, ABCA5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055156
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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