A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056570



Internal ID19145789
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 StatusM
Merged Variantsdgv3077n100
Supporting Variantsnssv3560054
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)nsv1056570
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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