A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015398



Internal ID21924741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139100766..139100819hg38UCSC Ensembl
chr7:138785512..138785565hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575464
Samples
Known GenesZC3HAV1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015398
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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