A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576087



Internal ID16016810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77272257..77276431hg38UCSC Ensembl
Innerchr17:75268339..75272513hg19UCSC Ensembl
Innerchr17:72779934..72784108hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg384175
hg194175
hg184175
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv876244
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576087
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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