A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699066



Internal ID15089032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:73994944..74031262hg38UCSC Ensembl
Innerchr17:71991083..72027401hg19UCSC Ensembl
Innerchr17:69502678..69538996hg18UCSC Ensembl
Innerchr17:69502678..69538996hg17UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3836319
hg1936319
hg1836319
hg1736319
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517569
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699066
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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