A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995531



Internal ID64464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44885764..44885818hg38UCSC Ensembl
chr7:44925363..44925417hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5488083
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995531
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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