A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200918



Internal ID20767958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156009526..156058387hg38UCSC Ensembl
chr1:155979317..156028178hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3848862
hg1948862
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6317671
Supporting Variants
Samples
Known GenesLAMTOR2, MIR7851, SSR2, UBQLN4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200918
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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