A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6002071



Internal ID21911414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138718201..138718293hg38UCSC Ensembl
chr7:138402946..138403038hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564424
Samples
Known GenesATP6V0A4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6002071
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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