A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324192



Internal ID20857317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:245282142..245286551hg38UCSC Ensembl
chr1:245445444..245449853hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg384410
hg194410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059706
Samples
Known GenesKIF26B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324192
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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