A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046097



Internal ID20613137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:28377231..29769380hg38UCSC Ensembl
chr19:28868138..30260287hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg381392150
hg191392150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6526233
Supporting Variants
Samples
Known GenesC19orf12, LINC00906, LOC100505835, LOC284395, PLEKHF1, POP4, UQCRFS1, VSTM2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046097
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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