A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3720021



Internal ID18671616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:21121674..21207107hg38UCSC Ensembl
Innerchr17:21024987..21110420hg19UCSC Ensembl
Innerchr17:20965579..21051012hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3885434
hg1985434
hg1885434
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059210
Supporting Variants
Samples
Known GenesDHRS7B, TMEM11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3720021
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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