A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360034



Internal ID21017587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:31177897..31204410hg38UCSC Ensembl
chr4:31179519..31206032hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3826514
hg1926514
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114814
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360034
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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