A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575551



Internal ID16362960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:51928604..51976841hg38UCSC Ensembl
Innerchr17:50005964..50054201hg19UCSC Ensembl
Innerchr17:47360963..47409200hg18UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg3848238
hg1948238
hg1848238
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv873538
Samples
Known GenesCA10
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575551
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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