A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326133



Internal ID20859267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62297596..62298354hg38UCSC Ensembl
chr1:62763268..62764026hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38759
hg19759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063422
Samples
Known GenesKANK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326133
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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