A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18074904



Internal ID20641944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:37287222..37834905hg38UCSC Ensembl
chr22:37683263..38230912hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38547684
hg19547650
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6540218
Supporting Variants
Samples
Known GenesANKRD54, CARD10, CDC42EP1, CYTH4, ELFN2, GALR3, GCAT, GGA1, H1F0, LGALS1, LGALS2, MFNG, NOL12, PDXP, SH3BP1, TRIOBP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18074904
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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