A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007998



Internal ID21917341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:124149718..124206646hg38UCSC Ensembl
chr6:124470863..124527791hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3856929
hg1956929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577238
Samples
Known GenesNKAIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007998
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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