A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604765



Internal ID16392174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139667879..140771106hg38UCSC Ensembl
Innerchr6:139989016..141092243hg19UCSC Ensembl
Innerchr6:140030709..141133936hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg381103228
hg191103228
hg181103228
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1073801
Samples
Known GenesLOC100132735, MIR3668, MIR4465
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604765
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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