A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332859



Internal ID20866034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244427301..244428200hg38UCSC Ensembl
chr1:244590603..244591502hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059636
Samples
Known GenesADSS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332859
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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