A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362270



Internal ID21019823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:63444727..63445368hg38UCSC Ensembl
chr3:63430403..63431044hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38642
hg19642
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18102462
Samples
Known GenesSYNPR, SYNPR-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362270
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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