A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6415879



Internal ID21073432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:152164564..152669678hg38UCSC Ensembl
chr7:151861649..152366763hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38505115
hg19505115
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231254
Samples
Known GenesFABP5P3, KMT2C, LINC01003, XRCC2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6415879
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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