A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv604977



Internal ID16392386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:156872116..156904910hg38UCSC Ensembl
Innerchr6:157193250..157226044hg19UCSC Ensembl
Innerchr6:157234942..157267736hg18UCSC Ensembl
Cytoband6q25.3
Allele length
AssemblyAllele length
hg3832795
hg1932795
hg1832795
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1074983
Samples
Known GenesARID1B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv604977
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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