A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604421



Internal ID16045144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:104813138..104843537hg38UCSC Ensembl
Innerchr6:105261013..105291412hg19UCSC Ensembl
Innerchr6:105367706..105398105hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg3830400
hg1930400
hg1830400
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1071843
Samples
Known GenesHACE1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604421
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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