A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327249



Internal ID20860386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47765303..47765918hg38UCSC Ensembl
chr1:48230975..48231590hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061623
Samples
Known GenesTRABD2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327249
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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