A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525034



Internal ID20898395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:51123901..51125600hg38UCSC Ensembl
chr19:51627158..51628857hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048706
Samples
Known GenesSIGLEC9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525034
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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