A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527484



Internal ID20900845
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44697442..44705349hg38UCSC Ensembl
chr19:45200712..45208619hg19UCSC Ensembl
Cytoband19q13.32
Allele length
AssemblyAllele length
hg387908
hg197908
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048189
Samples
Known GenesCEACAM16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527484
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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