A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615887



Internal ID20988958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88517053..90538988hg38UCSC Ensembl
chr7:88146368..90168302hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg382021936
hg192021935
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7001n223
Supporting Variantsnssv18221022
Samples
Known GenesC7orf62, C7orf63, CLDN12, DPY19L2P4, GTPBP10, LOC101409256, STEAP1, STEAP2, ZNF804B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615887
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer