A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575945



Internal ID16363354
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:70455366..70510541hg38UCSC Ensembl
Innerchr17:68451507..68506682hg19UCSC Ensembl
Innerchr17:65963102..66018277hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3855176
hg1955176
hg1855176
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5760n54
Supporting Variantsnssv875923
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575945
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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