A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447162



Internal ID21104715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63397563..63417873hg38UCSC Ensembl
chr10:65157323..65177633hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3820311
hg1920311
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982849
Samples
Known GenesJMJD1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447162
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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