A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6609994



Internal ID20983065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2531134..2535178hg38UCSC Ensembl
chr7:2570768..2574812hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg384045
hg194045
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155529
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6609994
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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