A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158142



Internal ID20725182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75767130..75802061hg38UCSC Ensembl
chr7:75396448..75431379hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3834932
hg1934932
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6617641
Supporting Variants
Samples
Known GenesCCL26
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158142
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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