A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431853



Internal ID21089406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137564449..137567524hg38UCSC Ensembl
chr7:137249195..137252270hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg383076
hg193076
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155152
Samples
Known GenesDGKI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431853
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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