A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020357



Internal ID18762892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160428863..160462362hg38UCSC Ensembl
Innerchr6:160849895..160883394hg19UCSC Ensembl
Innerchr6:160769885..160803384hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3833500
hg1933500
hg1833500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654495
Samples
Known GenesSLC22A3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020357
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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