A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16994173



Internal ID63566
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37676967..37738533hg38UCSC Ensembl
chr7:37716570..37778135hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3861567
hg1961566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5491110
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16994173
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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