A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6418456



Internal ID21076009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:40645001..40647000hg38UCSC Ensembl
chr8:40502520..40504519hg19UCSC Ensembl
Cytoband8p11.21
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18166853
Samples
Known GenesZMAT4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6418456
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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