A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323577



Internal ID20856696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21049901..21056200hg38UCSC Ensembl
chr1:21376394..21382693hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg386300
hg196300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199925
Samples
Known GenesEIF4G3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323577
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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