A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031548



Internal ID19120770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:63316957..63392140hg38UCSC Ensembl
Innerchr6:64026862..64102045hg19UCSC Ensembl
Innerchr6:64084821..64160004hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3875184
hg1975184
hg1875184
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5995n100
Supporting Variantsnssv3657647
Samples
Known GenesLGSN
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031548
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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