A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6030035



Internal ID21939378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:71565826..71565975hg38UCSC Ensembl
chr11:71276872..71277021hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg38150
hg19150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17594825
Samples
Known GenesKRTAP5-10
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6030035
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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