A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449848



Internal ID21107401
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:21768563..21786914hg38UCSC Ensembl
chr10:22057492..22075843hg19UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3818352
hg1918352
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979630
Samples
Known GenesDNAJC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449848
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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