A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866661



Internal ID16160617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:6070390..6071723hg38UCSC Ensembl
Innerchr17:5973710..5975043hg19UCSC Ensembl
Innerchr17:5914434..5915767hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg381334
hg191334
hg181334
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574311
Supporting Variants
Samples
Known GenesWSCD1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866661
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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