A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334866



Internal ID20868055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16370323..16373244hg38UCSC Ensembl
chr1:16696818..16699739hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg382922
hg192922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052618
Samples
Known GenesSZRD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334866
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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