A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18160762



Internal ID20727802
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96855428..96866658hg38UCSC Ensembl
chr7:96484740..96495970hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3811231
hg1911231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602120
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18160762
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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