A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334939



Internal ID20868129
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:235347920..235393001hg38UCSC Ensembl
chr1:235511235..235556316hg19UCSC Ensembl
Cytoband1q42.3
Allele length
AssemblyAllele length
hg3845082
hg1945082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058857
Samples
Known GenesTBCE
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334939
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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