A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6427446



Internal ID21084999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154544925..154549261hg38UCSC Ensembl
chr7:154242010..154246346hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg384337
hg194337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154186
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6427446
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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