A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6015282



Internal ID21924625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76515456..77046723hg38UCSC Ensembl
chr7:76144773..76676040hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38531268
hg19531268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563470
Samples
Known GenesDTX2P1-UPK3BP1-PMS2P11, LOC100132832, LOC100133091, POMZP3, UPK3B
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6015282
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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