A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17006018



Internal ID71627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157262179..158261000hg38UCSC Ensembl
chr7:157054873..158053692hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38998822
hg19998820
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5563018
Supporting Variants
Samples
Known GenesDNAJB6, LOC100506585, MIR153-2, PTPRN2, UBE3C
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17006018
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequency0.000312


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