A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006380



Internal ID21915723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:125788031..126223767hg38UCSC Ensembl
chr7:125428085..125863821hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38435737
hg19435737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17568478
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006380
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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