A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15752649



Internal ID21388943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:180286171..180286723hg38UCSC Ensembl
chr5:179713171..179713723hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg38553
hg19553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434594
Supporting Variants
SamplesNB08
Known GenesMAPK9
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15752649
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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