A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153700



Internal ID20720740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35817901..35819800hg38UCSC Ensembl
chr7:35857511..35859410hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg381900
hg191900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6616946
Supporting Variants
Samples
Known GenesSEPT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153700
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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