A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576077



Internal ID16016800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77264304..77297220hg38UCSC Ensembl
Innerchr17:75260386..75293302hg19UCSC Ensembl
Innerchr17:72771981..72804897hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3832917
hg1932917
hg1832917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv876230
Samples
Known GenesSEPT9
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576077
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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