A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6387634



Internal ID21045187
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:102921488..103773850hg38UCSC Ensembl
chr4:103842645..104695007hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg38852363
hg19852363
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209450
Samples
Known GenesBDH2, CENPE, SLC9B1, SLC9B2, TACR3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6387634
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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