A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16909484



Internal ID7106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:11220172..11220281hg38UCSC Ensembl
chr2:11360298..11360407hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5443033
Supporting Variants
Samples
Known GenesROCK2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16909484
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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