A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6422865



Internal ID21080418
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157138401..157139400hg38UCSC Ensembl
chr7:156931095..156932094hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151502
Samples
Known GenesUBE3C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6422865
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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