A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316070



Internal ID20849147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:29177426..29180495hg38UCSC Ensembl
chr1:29503938..29507007hg19UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg383070
hg193070
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060004
Samples
Known GenesSRSF4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316070
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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