A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432153



Internal ID21089706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:133455084..133629013hg38UCSC Ensembl
chr7:133139838..133313766hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38173930
hg19173929
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151605
Samples
Known GenesEXOC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432153
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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