A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18159514



Internal ID20726554
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74179688..74183754hg38UCSC Ensembl
chr7:73594018..73598084hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg384067
hg194067
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608082
Supporting Variants
Samples
Known GenesEIF4H
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18159514
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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