A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575730



Internal ID16363139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:57131143..57132634hg38UCSC Ensembl
Innerchr17:55208504..55209995hg19UCSC Ensembl
Innerchr17:52563503..52564994hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381492
hg191492
hg181492
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv874404
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575730
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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