A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431454



Internal ID21089007
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137054001..137058000hg38UCSC Ensembl
chr7:136738748..136742747hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154423
Samples
Known GenesLOC349160
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431454
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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