A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv875846



Internal ID16169802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:66292519..66299570hg38UCSC Ensembl
Innerchr17:64288637..64295688hg19UCSC Ensembl
Innerchr17:61719099..61726150hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg387052
hg197052
hg187052
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575893
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)nssv875846
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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