A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6530727



Internal ID20904088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42507761..42510937hg38UCSC Ensembl
chr19:43011913..43015089hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg383177
hg193177
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046406
Samples
Known GenesCEACAM1, LIPE-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6530727
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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