A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695102



Internal ID15431754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68677651..68687038hg38UCSC Ensembl
Innerchr17:66673792..66683179hg19UCSC Ensembl
Innerchr17:64185387..64194774hg18UCSC Ensembl
Innerchr17:64185387..64194774hg17UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg389388
hg199388
hg189388
hg179388
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522322
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695102
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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