A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524061



Internal ID8418336
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31139310..31166166hg38UCSC Ensembl
Innerchr6:31107087..31133943hg19UCSC Ensembl
Innerchr6:31215066..31241922hg18UCSC Ensembl
Innerchr6:31215066..31241922hg17UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg3826857
hg1926857
hg1826857
hg1726857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699927
Samples
Known GenesCCHCR1, POU5F1, PSORS1C1, PSORS1C2, TCF19
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524061
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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