A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604095



Internal ID16391504
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:85867136..85938718hg38UCSC Ensembl
Innerchr6:86576854..86648436hg19UCSC Ensembl
Innerchr6:86633573..86705155hg18UCSC Ensembl
Cytoband6q14.3
Allele length
AssemblyAllele length
hg3871583
hg1971583
hg1871583
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10829n54
Supporting Variantsnssv1154844
Samples1780854039_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604095
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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