A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv673306



Internal ID15063272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:36459737..36534535hg38UCSC Ensembl
Innerchr17:34815551..34890362hg19UCSC Ensembl
Innerchr17:31889664..31964475hg18UCSC Ensembl
Innerchr17:31889664..31964475hg17UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3874799
hg1974812
hg1874812
hg1774812
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516100
Supporting Variants
Samples
Known GenesMYO19, ZNHIT3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv673306
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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