A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151434



Internal ID20718474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156165001..156165900hg38UCSC Ensembl
chr7:155957695..155958594hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418973
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151434
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0045


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