A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453638



Internal ID21111191
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:95212645..95230076hg38UCSC Ensembl
chr10:96972402..96989833hg19UCSC Ensembl
Cytoband10q23.33
Allele length
AssemblyAllele length
hg3817432
hg1917432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985728
Samples
Known GenesC10orf129
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453638
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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