A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv603190



Internal ID16043913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:57109104..57234175hg38UCSC Ensembl
Innerchr6:56973902..57098973hg19UCSC Ensembl
Innerchr6:57081861..57206932hg18UCSC Ensembl
Cytoband6p11.2
Allele length
AssemblyAllele length
hg38125072
hg19125072
hg18125072
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1154086
Samples1780862206_A
Known GenesBAG2, RAB23, ZNF451
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv603190
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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