A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18161740



Internal ID20728780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87153450..87157221hg38UCSC Ensembl
chr7:86782766..86786537hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg383772
hg193772
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617350
Supporting Variants
Samples
Known GenesDMTF1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18161740
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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