A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6516045



Internal ID20889406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:3541413..3552500hg38UCSC Ensembl
chr19:3541411..3552498hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg3811088
hg1911088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046286
Samples
Known GenesC19orf71, MFSD12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6516045
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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