A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16995192



Internal ID64223
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41719014..41719777hg38UCSC Ensembl
chr7:41758612..41759375hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38764
hg19764
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5486084
Supporting Variants
Samples
Known GenesINHBA-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16995192
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.002185


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