A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320981



Internal ID20854082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175057101..175126400hg38UCSC Ensembl
chr1:175026237..175095536hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3869300
hg1969300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201056
Samples
Known GenesTNN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320981
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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