A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618026



Internal ID20991097
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12483629..12673529hg38UCSC Ensembl
chr7:12523255..12713154hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38189901
hg19189900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6580n223
Supporting Variantsnssv18150220
Samples
Known GenesSCIN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618026
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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