A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523301



Internal ID15103908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:54031357..54056329hg38UCSC Ensembl
Innerchr6:53896155..53921127hg19UCSC Ensembl
Innerchr6:54004114..54029086hg18UCSC Ensembl
Innerchr6:54004114..54029086hg17UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3824973
hg1924973
hg1824973
hg1724973
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699041
Samples
Known GenesMLIP
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523301
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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