A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576036



Internal ID16016759
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 StatusM
Merged Variantsdgv5776n54
Supporting Variantsnssv876112, nssv876111
Samples
Known GenesITGB4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576036
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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