A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6377908



Internal ID21035461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:57697464..58703214hg38UCSC Ensembl
chr4:58563630..59569379hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg381005751
hg191005750
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212556
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6377908
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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