A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447648



Internal ID21105201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:102764568..102766379hg38UCSC Ensembl
chr10:104524325..104526136hg19UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg381812
hg191812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977273
Samples
Known GenesWBP1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447648
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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