A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18111711



Internal ID20678751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:159124267..159129936hg38UCSC Ensembl
chr4:160045419..160051088hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg385670
hg195670
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6384929
Supporting Variants
Samples
Known GenesMIR3688-1, MIR3688-2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18111711
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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