A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18201822



Internal ID20768863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:202173734..202204798hg38UCSC Ensembl
chr1:202142862..202173926hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3831065
hg1931065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6321694
Supporting Variants
Samples
Known GenesLGR6, PTPRVP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18201822
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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