A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522773



Internal ID8417048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:160731417..160749803hg38UCSC Ensembl
Innerchr6:161152449..161170835hg19UCSC Ensembl
Innerchr6:161072439..161090825hg18UCSC Ensembl
Innerchr6:161122860..161141246hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3818387
hg1918387
hg1818387
hg1718387
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698414
Samples
Known GenesPLG
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522773
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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