A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6527548



Internal ID20900909
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:10403327..10404560hg38UCSC Ensembl
chr19:10514003..10515236hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381234
hg191234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18044301
Samples
Known GenesCDC37, MIR1181
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6527548
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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