A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325543



Internal ID20858674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16408869..16430120hg38UCSC Ensembl
chr1:16735364..16756615hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3821252
hg1921252
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201916
Samples
Known GenesSPATA21
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325543
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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