A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330127



Internal ID20863281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:8402451..8411533hg38UCSC Ensembl
chr1:8462511..8471593hg19UCSC Ensembl
Cytoband1p36.23
Allele length
AssemblyAllele length
hg389083
hg199083
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064394
Samples
Known GenesRERE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330127
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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