A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3567724



Internal ID18519319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:63478305..63514291hg38UCSC Ensembl
Innerchr17:61555666..61591652hg19UCSC Ensembl
Innerchr17:58909398..58945384hg18UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3835987
hg1935987
hg1835987
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1055722
Supporting Variants
Samples
Known GenesACE
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3567724
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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