A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202081



Internal ID20769122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:57948090..58009516hg38UCSC Ensembl
chr1:58413762..58475188hg19UCSC Ensembl
Cytoband1p32.2
Allele length
AssemblyAllele length
hg3861427
hg1961427
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6330537
Supporting Variants
Samples
Known GenesDAB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202081
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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