A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331495



Internal ID20864659
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:238367766..238568387hg38UCSC Ensembl
chr1:238531066..238731687hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg38200622
hg19200622
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18059289
Samples
Known GenesLINC01139
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331495
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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