A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318559



Internal ID20851651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58841692..58845409hg38UCSC Ensembl
chr1:59307364..59311081hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg383718
hg193718
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061926
Samples
Known GenesLINC01135
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318559
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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