A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440005



Internal ID21097558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48666829..48668769hg38UCSC Ensembl
chr10:49874874..49876814hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg381941
hg191941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979990
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440005
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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