A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18202500



Internal ID20769540
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:237853292..237936050hg38UCSC Ensembl
chr1:238016592..238099350hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3882759
hg1982759
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6334863
Supporting Variants
Samples
Known GenesLOC100130331, ZP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18202500
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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