A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18190592



Internal ID20757632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:78892284..78969688hg38UCSC Ensembl
chr10:80652041..80729445hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg3877405
hg1977405
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6441889
Supporting Variants
Samples
Known GenesZMIZ1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18190592
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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