A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6319283



Internal ID20852376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:55156301..55157300hg38UCSC Ensembl
chr1:55621974..55622973hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062205
Samples
Known GenesUSP24
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6319283
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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