A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689704



Internal ID15079670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9227001..9238006hg38UCSC Ensembl
Innerchr17:9130318..9141323hg19UCSC Ensembl
Innerchr17:9071043..9082048hg18UCSC Ensembl
Innerchr17:9071043..9082048hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3811006
hg1911006
hg1811006
hg1711006
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521247
Supporting Variants
Samples
Known GenesNTN1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689704
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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