A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424090



Internal ID21081643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:37737128..37738419hg38UCSC Ensembl
chr8:37594646..37595937hg19UCSC Ensembl
Cytoband8p11.23
Allele length
AssemblyAllele length
hg381292
hg191292
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18168900
Samples
Known GenesERLIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424090
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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