A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001444



Internal ID68559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119211223..119392959hg38UCSC Ensembl
chr7:118851277..119033013hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38181737
hg19181737
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5474364
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001444
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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