A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17982572



Internal ID20549612
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:6149499..6156984hg38UCSC Ensembl
chr10:6191462..6198947hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg387486
hg197486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6439124
Supporting Variants
Samples
Known GenesMIR3155A, MIR3155B, PFKFB3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17982572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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