A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6042611



Internal ID21951927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:30809168..31168586hg38UCSC Ensembl
chr21:32181486..32540903hg19UCSC Ensembl
Cytoband21q22.11
Allele length
AssemblyAllele length
hg38359419
hg19359418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17645199
Samples
Known GenesKRTAP11-1, KRTAP19-8, KRTAP7-1, KRTAP8-1, TIAM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6042611
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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