A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004142



Internal ID21913485
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36448480..36452556hg38UCSC Ensembl
chr6:36416257..36420333hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg384077
hg194077
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565682
Samples
Known GenesKCTD20
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004142
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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