A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5434735



Internal ID213404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:213190336..213190446hg38UCSC Ensembl
chr2:214055060..214055170hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg38111
hg19111
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16923759
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5434735
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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