A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5903934



Internal ID22679107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135313247..135321913hg38UCSC Ensembl
chr2:136070817..136079483hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg388667
hg198667
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17401942
Samples
Known GenesZRANB3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5903934
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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