A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325376



Internal ID20858507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2652001..2683100hg38UCSC Ensembl
chr1:2583440..2614539hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3831100
hg1931100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv33n223
Supporting Variantsnssv18203477
Samples
Known GenesTTC34
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325376
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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