A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6602960



Internal ID20976031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:80965281..80967596hg38UCSC Ensembl
chr7:80594597..80596912hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg382316
hg192316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18160849
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6602960
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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