A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608507



Internal ID20981578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:3143360..3149323hg38UCSC Ensembl
chr7:3182994..3188957hg19UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg385964
hg195964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156025
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608507
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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