A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415969



Internal ID21073522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105554701..105555600hg38UCSC Ensembl
chr8:106566929..106567828hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18162292
Samples
Known GenesZFPM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415969
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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