A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452682



Internal ID21110235
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:49484401..49489816hg38UCSC Ensembl
chr10:50692447..50697862hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg385416
hg195416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980023
Samples
Known GenesERCC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452682
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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