A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1077400



Internal ID15930586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170085964..170087974hg38UCSC Ensembl
Innerchr6:170401188..170403198hg19UCSC Ensembl
Innerchr6:170243113..170245123hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382011
hg192011
hg182011
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv605535
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1077400
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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