A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567812



Internal ID18519407
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77118623..77628815hg38UCSC Ensembl
Innerchr17:75114705..75624897hg19UCSC Ensembl
Innerchr17:72626300..73136492hg18UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg38510193
hg19510193
hg18510193
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061331
Supporting Variants
Samples
Known GenesLOC100507351, MIR4316, SEC14L1, SEPT9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567812
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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