A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6431268



Internal ID21088821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158408734..158834438hg38UCSC Ensembl
chr7:158201426..158627129hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38425705
hg19425704
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7205n223
Supporting Variantsnssv18219201
Samples
Known GenesESYT2, MIR5707, MIR595, NCAPG2, PTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6431268
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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