A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16998251



Internal ID66380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71387209..71387277hg38UCSC Ensembl
chr7:70852195..70852263hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5485763
Supporting Variants
Samples
Known GenesWBSCR17
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16998251
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.001249


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