A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18200932



Internal ID20767972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156967197..156967990hg38UCSC Ensembl
chr1:156936989..156937782hg19UCSC Ensembl
Cytoband1q23.1
Allele length
AssemblyAllele length
hg38794
hg19794
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319004
Supporting Variants
Samples
Known GenesARHGEF11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18200932
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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