A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526180



Internal ID20899541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44220089..44221051hg38UCSC Ensembl
chr19:44724242..44725204hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38963
hg19963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048150
Samples
Known GenesZNF227
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526180
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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