A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18211728



Internal ID20778768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:70931350..70954532hg38UCSC Ensembl
chr4:71797067..71820249hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3823183
hg1923183
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6387096
Supporting Variants
Samples
Known GenesMOB1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18211728
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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