A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335193



Internal ID20868385
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:179638152..179638924hg38UCSC Ensembl
chr1:179607287..179608059hg19UCSC Ensembl
Cytoband1q25.2
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053991
Samples
Known GenesTDRD5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335193
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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