A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6389560



Internal ID21047113
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:37856189..37895442hg38UCSC Ensembl
chr4:37857810..37897063hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3839254
hg1939254
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18115984
Samples
Known GenesPGM2, TBC1D1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6389560
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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