A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv873561



Internal ID16167517
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:53446686..53497253hg38UCSC Ensembl
Innerchr17:51524047..51574614hg19UCSC Ensembl
Innerchr17:48879046..48929613hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3850568
hg1950568
hg1850568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575577
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv873561
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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