A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447541



Internal ID21105094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122896201..122897700hg38UCSC Ensembl
chr10:124655717..124657216hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978238
Samples
Known GenesLOC399815
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447541
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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