A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16994164



Internal ID63558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37600465..37600977hg38UCSC Ensembl
chr7:37640068..37640580hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38513
hg19513
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5490428
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16994164
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000624


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