A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6519984



Internal ID20893345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:45832375..45835838hg38UCSC Ensembl
chr18:43412340..43415803hg19UCSC Ensembl
Cytoband18q12.3
Allele length
AssemblyAllele length
hg383464
hg193464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18041886
Samples
Known GenesSIGLEC15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6519984
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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