A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319634



Internal ID20852729
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:153887864..153890619hg38UCSC Ensembl
chr1:153860340..153863095hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382756
hg192756
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052002
Samples
Known GenesGATAD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319634
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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