A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337881



Internal ID20995434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:135380652..135394441hg38UCSC Ensembl
chr2:136138222..136152011hg19UCSC Ensembl
Cytoband2q21.3
Allele length
AssemblyAllele length
hg3813790
hg1913790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077887
Samples
Known GenesZRANB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337881
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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