A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6416958



Internal ID21074511
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:724476..896551hg38UCSC Ensembl
chr8:674476..846551hg19UCSC Ensembl
Cytoband8p23.3
Allele length
AssemblyAllele length
hg38172076
hg19172076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170318
Samples
Known GenesERICH1, ERICH1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6416958
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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