A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604230



Internal ID16391639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:94830882..94939749hg38UCSC Ensembl
Innerchr6:95540600..95649467hg19UCSC Ensembl
Innerchr6:95597321..95706188hg18UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg38108868
hg19108868
hg18108868
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10857n54
Supporting Variantsnssv1069233
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604230
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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