A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614039



Internal ID20987110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102062723..102064035hg38UCSC Ensembl
chr7:101706003..101707315hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381313
hg191313
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151240
Samples
Known GenesCUX1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614039
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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