A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17000556



Internal ID67949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103099256..103105142hg38UCSC Ensembl
chr7:102739703..102745589hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg385887
hg195887
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5475533
Supporting Variants
Samples
Known GenesARMC10, NAPEPLD
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17000556
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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