A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18151461



Internal ID20718501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156537362..156546008hg38UCSC Ensembl
chr7:156330056..156338702hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg388647
hg198647
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6418606
Supporting Variants
Samples
Known GenesLINC00244, LINC01006
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18151461
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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