A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6330606



Internal ID20863764
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32688025..32689202hg38UCSC Ensembl
chr1:33153626..33154803hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg381178
hg191178
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203609
Samples
Known GenesSYNC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6330606
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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