A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323519



Internal ID20856637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15845401..15849500hg38UCSC Ensembl
chr1:16171896..16175995hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg384100
hg194100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200948
Samples
Known GenesFLJ37453, SPEN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323519
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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