A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv872936



Internal ID15820206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46588633..46687409hg38UCSC Ensembl
Innerchr17:44665999..44764775hg19UCSC Ensembl
Innerchr17:42021315..42119955hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3898777
hg1998777
hg1898641
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv575409
Supporting Variants
Samples
Known GenesNSF, NSFP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv872936
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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