A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6036311



Internal ID21945654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:70106881..70108298hg38UCSC Ensembl
chr17:68103022..68104439hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg381418
hg191418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631750
Samples
Known GenesKCNJ16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6036311
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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