A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431148



Internal ID21088701
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:23287135..23460409hg38UCSC Ensembl
chr8:23144648..23317922hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38173275
hg19173275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18167130
Samples
Known GenesENTPD4, LOC100507156, LOXL2, R3HCC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431148
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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