A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201040



Internal ID20768080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:174087067..174094078hg38UCSC Ensembl
chr1:174056205..174063216hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg387012
hg197012
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317197
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201040
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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