A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331376



Internal ID20864539
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:102852101..102858800hg38UCSC Ensembl
chr1:103317657..103324356hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg386700
hg196700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200317
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331376
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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