A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv866760



Internal ID15814030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9148000..9504608hg38UCSC Ensembl
Innerchr17:9051317..9407925hg19UCSC Ensembl
Innerchr17:8992042..9348650hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg38356609
hg19356609
hg18356609
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv574341
Supporting Variants
Samples
Known GenesNTN1, STX8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv866760
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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