A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153339



Internal ID20720379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:129130183..129132270hg38UCSC Ensembl
chr7:128770237..128772324hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg382088
hg192088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427053
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153339
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00116


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