A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18235959



Internal ID20802999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158440601..158595400hg38UCSC Ensembl
chr7:158233293..158388092hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38154800
hg19154800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6431394
Supporting Variants
Samples
Known GenesMIR5707, MIR595, PTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18235959
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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