A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370369



Internal ID21027922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44845226..44845794hg38UCSC Ensembl
chr3:44886718..44887286hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100622
Samples
Known GenesKIF15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370369
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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