A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18206972



Internal ID20774012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68136268..68136653hg38UCSC Ensembl
chr2:68363400..68363785hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38386
hg19386
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6352714
Supporting Variants
Samples
Known GenesWDR92
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18206972
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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