A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16993254



Internal ID62955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:6998000..7111000hg38UCSC Ensembl
chr7:7037631..7150631hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38113001
hg19113001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5467055
Supporting Variants
Samples
Known GenesLOC100131257
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16993254
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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