A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6007521



Internal ID21916864
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139424850..139425216hg38UCSC Ensembl
chr7:139109596..139109962hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38367
hg19367
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17562994
Samples
Known GenesLOC100129148
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6007521
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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