A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322113



Internal ID20855223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:200612254..200624658hg38UCSC Ensembl
chr1:200581382..200593786hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3812405
hg1912405
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056903
Samples
Known GenesKIF14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322113
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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