A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17006909



Internal ID72222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156522913..156529153hg38UCSC Ensembl
chr7:156315607..156321847hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg386241
hg196241
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5484778
Supporting Variants
Samples
Known GenesLINC01006
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17006909
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000156


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