A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371067



Internal ID21028620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:57762723..57769200hg38UCSC Ensembl
chr3:57748450..57754927hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg386478
hg196478
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212286
Samples
Known GenesSLMAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371067
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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