A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326623



Internal ID20859760
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:175099701..175126200hg38UCSC Ensembl
chr1:175068837..175095336hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg3826500
hg1926500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv442n223
Supporting Variantsnssv18201062
Samples
Known GenesTNN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326623
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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