A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3560054



Internal ID18858335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:832061..887888hg38UCSC Ensembl
Innerchr17:735301..791128hg19UCSC Ensembl
Innerchr17:682051..737878hg18UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3855828
hg1955828
hg1855828
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1056570
Supporting Variants
Samples
Known GenesNXN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3560054
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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