A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6017618



Internal ID21926961
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:99426614..99426965hg38UCSC Ensembl
chr7:99024237..99024588hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38352
hg19352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558427
Samples
Known GenesATP5J2-PTCD1, PTCD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6017618
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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