A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6455583



Internal ID21113136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130983601..131184500hg38UCSC Ensembl
chr10:132781864..132982763hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg38200900
hg19200900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv912n223
Supporting Variantsnssv18182824
Samples
Known GenesTCERG1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6455583
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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