A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154546



Internal ID20721586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:43153436..43153657hg38UCSC Ensembl
chr7:43193035..43193256hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619251
Supporting Variants
Samples
Known GenesHECW1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00176


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