A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151196



Internal ID20718236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121363330..121363695hg38UCSC Ensembl
chr7:121003384..121003749hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg38366
hg19366
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610136
Supporting Variants
Samples
Known GenesFAM3C
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00102


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