A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17439350



Internal ID22497220
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:43067621..43068289hg38UCSC Ensembl
chr6:43035359..43036027hg19UCSC Ensembl
Cytoband6p21.1
Allele length
AssemblyAllele length
hg38669
hg19669
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5890291
Supporting Variants
Samples
Known GenesKLC4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17439350
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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