A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv688335



Internal ID15078301
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9227001..9242651hg38UCSC Ensembl
Innerchr17:9130318..9145968hg19UCSC Ensembl
Innerchr17:9071043..9086693hg18UCSC Ensembl
Innerchr17:9071043..9086693hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3815651
hg1915651
hg1815651
hg1715651
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)nssv688335
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer