A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151072



Internal ID20718112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119589201..119596000hg38UCSC Ensembl
chr7:119229255..119236054hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6603990
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151072
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00292


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