A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17001604



Internal ID68673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:106093547..106093882hg38UCSC Ensembl
chr7:105733993..105734328hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg38336
hg19336
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5478924
Supporting Variants
Samples
Known GenesSYPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17001604
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.328442


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