A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv876111



Internal ID15823381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:75724647..75731974hg38UCSC Ensembl
Innerchr17:73720727..73728055hg19UCSC Ensembl
Innerchr17:71232322..71239650hg18UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg387328
hg197329
hg187329
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576036
Supporting Variants
Samples
Known GenesITGB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv876111
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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