A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150663



Internal ID20717703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14021601..14023200hg38UCSC Ensembl
chr7:14061226..14062825hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619693
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150663
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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