A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316595



Internal ID20849675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:21793645..21800277hg38UCSC Ensembl
chr1:22120138..22126770hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg386633
hg196633
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200588
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316595
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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