A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151977



Internal ID20719017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104389867..104389969hg38UCSC Ensembl
chr7:104030315..104030417hg19UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6605217
Supporting Variants
Samples
Known GenesLHFPL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151977
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00458


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