A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430946



Internal ID21088499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:87183882..87196683hg38UCSC Ensembl
chr8:88196110..88208911hg19UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3812802
hg1912802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18170924
Samples
Known GenesCNBD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430946
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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