A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326949



Internal ID20860086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:229339487..229339847hg38UCSC Ensembl
chr1:229475234..229475594hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202748
Samples
Known GenesCCSAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326949
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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