A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6495675



Internal ID20868869
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:51697177..51697290hg38UCSC Ensembl
chr15:51989374..51989487hg19UCSC Ensembl
Cytoband15q21.2
Allele length
AssemblyAllele length
hg38114
hg19114
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18024033
Samples
Known GenesSCG3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6495675
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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