A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv876222



Internal ID15823492
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77049144..77089240hg38UCSC Ensembl
Innerchr17:75045226..75085322hg19UCSC Ensembl
Innerchr17:72556821..72596917hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg3840097
hg1940097
hg1840097
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv576071
Supporting Variants
Samples
Known GenesLINC00338, SEC14L1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv876222
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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