A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601301



Internal ID20974372
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144558774..144560051hg38UCSC Ensembl
chr6:144879910..144881187hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg381278
hg191278
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18140286
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601301
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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