A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323911



Internal ID20857034
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:201956764..201957868hg38UCSC Ensembl
chr1:201925892..201926996hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381105
hg191105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056652
Samples
Known GenesTIMM17A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323911
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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