A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324609



Internal ID20857737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33011636..33015168hg38UCSC Ensembl
chr1:33477237..33480769hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg383533
hg193533
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060950
Samples
Known GenesAK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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