A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6434265



Internal ID21091818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154065854..154250480hg38UCSC Ensembl
chr7:153762939..153947565hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg38184627
hg19184627
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18230284
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6434265
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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