A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1155793



Internal ID15530187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149434559..149477699hg38UCSC Ensembl
Innerchr6:149755695..149798835hg19UCSC Ensembl
Innerchr6:149797388..149840528hg18UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3843141
hg1943141
hg1843141
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv604846
Supporting Variants
SamplesHGDP00907
Known GenesZC3H12D
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1155793
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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