A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6006870



Internal ID21916213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63245692..63245778hg38UCSC Ensembl
chr10:65005452..65005538hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3887
hg1987
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17581186
Samples
Known GenesJMJD1C
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6006870
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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