A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152009



Internal ID20719049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104727301..104730200hg38UCSC Ensembl
chr7:104367748..104370647hg19UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613333
Supporting Variants
Samples
Known GenesLHFPL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00013


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