A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440840



Internal ID21098393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125705634..125708244hg38UCSC Ensembl
chr10:127394203..127396813hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg382611
hg192611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978644
Samples
Known GenesFLJ37035, LOC283038
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440840
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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