A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605244



Internal ID16392653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:164880451..164917062hg38UCSC Ensembl
Innerchr6:165293940..165330551hg19UCSC Ensembl
Innerchr6:165213930..165250541hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3836612
hg1936612
hg1836612
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1075801
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605244
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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