A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875926



Internal ID16169882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:71187813..71236942hg38UCSC Ensembl
Innerchr17:69183954..69233083hg19UCSC Ensembl
Innerchr17:66695549..66744678hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3849130
hg1949130
hg1849130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575949
Supporting Variants
Samples
Known GenesCASC17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv875926
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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