A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150725



Internal ID20717765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140919301..140923300hg38UCSC Ensembl
chr7:140619101..140623100hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6427516
Supporting Variants
Samples
Known GenesBRAF
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150725
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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