A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618540



Internal ID20991611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:67243401..67383800hg38UCSC Ensembl
chr7:66708388..66848787hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38140400
hg19140400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158060
Samples
Known GenesLOC101929736, PMS2P4, STAG3L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618540
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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