A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121670



Internal ID20688710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:8585096..8588002hg38UCSC Ensembl
chr4:8586823..8589729hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg382907
hg192907
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6375260
Supporting Variants
Samples
Known GenesGPR78
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121670
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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