A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6426781



Internal ID21084334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:143707640..143976091hg38UCSC Ensembl
chr8:144789810..145050259hg19UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg38268452
hg19260450
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236391
Samples
Known GenesCCDC166, EPPK1, FAM83H, FAM83H-AS1, MAPK15, MIR4664, MIR661, MIR6845, MIR937, NRBP2, PLEC, PUF60, SCRIB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6426781
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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