A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444804



Internal ID21102357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:11017201..11018800hg38UCSC Ensembl
chr10:11059164..11060763hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979488
Samples
Known GenesCELF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444804
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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