A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6005414



Internal ID21914757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:985334..1041327hg38UCSC Ensembl
chr7:1024970..1080963hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3855994
hg1955994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562712
Samples
Known GenesC7orf50, CYP2W1, MIR339
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6005414
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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