A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6391355



Internal ID21048908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37344932..37353363hg38UCSC Ensembl
chr4:37346554..37354985hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg388432
hg198432
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115952
Samples
Known GenesKIAA1239
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6391355
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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