A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605376



Internal ID20978447
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144464501..144473300hg38UCSC Ensembl
chr6:144785637..144794436hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg388800
hg198800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18216933
Samples
Known GenesUTRN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605376
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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