A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18207048



Internal ID20774088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:74161609..74164478hg38UCSC Ensembl
chr2:74388736..74391605hg19UCSC Ensembl
Cytoband2p13.1
Allele length
AssemblyAllele length
hg382870
hg192870
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6347460
Supporting Variants
Samples
Known GenesMOB1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18207048
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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