A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150790



Internal ID20717830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141930680..141931276hg38UCSC Ensembl
chr7:141630480..141631076hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38597
hg19597
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6425265
Supporting Variants
Samples
Known GenesCLEC5A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150790
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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