A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16906602



Internal ID5186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:7715036..7720943hg38UCSC Ensembl
chr1:7775096..7781003hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg385908
hg195908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5419931
Supporting Variants
Samples
Known GenesCAMTA1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16906602
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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