A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604231



Internal ID16391640
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94834615..94925777hg38UCSC Ensembl
Innerchr6:95544333..95635495hg19UCSC Ensembl
Innerchr6:95601054..95692216hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3891163
hg1991163
hg1891163
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10857n54
Supporting Variantsnssv1069234
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604231
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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