A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377057



Internal ID21034610
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:112374701..112382900hg38UCSC Ensembl
chr4:113295857..113304056hg19UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg388200
hg198200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209546
Samples
Known GenesALPK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377057
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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