A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001159



Internal ID21910502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99517332..99519544hg38UCSC Ensembl
chr7:99114955..99117167hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg382213
hg192213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17577519
Samples
Known GenesZKSCAN5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001159
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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