A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15179504



Internal ID21318300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38217260..38217416hg38UCSC Ensembl
chr22:38613267..38613423hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg38157
hg19157
Variant TypeCNV deletion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3936055
Supporting Variants
SamplesHG002
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nssv15179504
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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