A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362130



Internal ID21019683
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:101324201..101325100hg38UCSC Ensembl
chr3:101043045..101043944hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092384
Samples
Known GenesSENP7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362130
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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