A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360612



Internal ID21018165
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:23082826..23095634hg38UCSC Ensembl
chr4:23084449..23097257hg19UCSC Ensembl
Cytoband4p15.2
Allele length
AssemblyAllele length
hg3812809
hg1912809
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360612
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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