A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6420142



Internal ID21077695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:38923995..38930264hg38UCSC Ensembl
chr8:38781513..38787782hg19UCSC Ensembl
Cytoband8p11.22
Allele length
AssemblyAllele length
hg386270
hg196270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168990
Samples
Known GenesPLEKHA2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6420142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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