A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018599



Internal ID18761132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:123187871..124008918hg38UCSC Ensembl
Innerchr6:123509016..124330063hg19UCSC Ensembl
Innerchr6:123550715..124371762hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38821048
hg19821048
hg18821048
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654345, nssv3654346, nssv3654347
Samples
Known GenesNKAIN2, TRDN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018599
Frequency
Sample Size29084
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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