A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322008



Internal ID20855117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:28216201..28219500hg38UCSC Ensembl
chr1:28542712..28546011hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg383300
hg193300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059719
Samples
Known GenesDNAJC8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322008
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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