A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323499



Internal ID20856617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8635121..8655821hg38UCSC Ensembl
chr1:8695180..8715880hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg3820701
hg1920701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18065514
Samples
Known GenesRERE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323499
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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