A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317073



Internal ID20850157
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:225008258..225009989hg38UCSC Ensembl
chr1:225195960..225197691hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg381732
hg191732
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058309
Samples
Known GenesDNAH14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317073
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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