A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604753



Internal ID16392162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139282607..139295399hg38UCSC Ensembl
Innerchr6:139603744..139616536hg19UCSC Ensembl
Innerchr6:139645437..139658229hg18UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3812793
hg1912793
hg1812793
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1073764
Samples
Known GenesTXLNB
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604753
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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