A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604133



Internal ID16391542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91286018..91408059hg38UCSC Ensembl
Innerchr6:91995736..92117777hg19UCSC Ensembl
Innerchr6:92052457..92174498hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38122042
hg19122042
hg18122042
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10838n54
Supporting Variantsnssv1068400
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604133
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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