A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15749273



Internal ID21391369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180286147..180286723hg38UCSC Ensembl
chr5:179713147..179713723hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38577
hg19577
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434593
Supporting Variants
SamplesNB12
Known GenesMAPK9
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15749273
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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