A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576188



Internal ID16016911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:82047894..82065174hg38UCSC Ensembl
Innerchr17:80005770..80023050hg19UCSC Ensembl
Innerchr17:77599059..77616339hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3817281
hg1917281
hg1817281
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877121
Samples
Known GenesDUS1L, GPS1, RFNG
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576188
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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