A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6419859



Internal ID21077412
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:142714458..142854276hg38UCSC Ensembl
chr8:143795876..143935692hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38139819
hg19139817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167370
Samples
Known GenesGML, LOC100288181, LY6D, LYNX1, LYPD2, SLURP1, THEM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6419859
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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