A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575552



Internal ID16362961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:51941954..51997028hg38UCSC Ensembl
Innerchr17:50019314..50074388hg19UCSC Ensembl
Innerchr17:47374313..47429387hg18UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3855075
hg1955075
hg1855075
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv873539
Samples
Known GenesCA10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575552
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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