A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444972



Internal ID21102525
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63270239..63271666hg38UCSC Ensembl
chr10:65029999..65031426hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381428
hg191428
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17982835
Samples
Known GenesJMJD1C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444972
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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