A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244729



Internal ID21306906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:30500366..30796274hg38UCSC Ensembl
Outerchr15:30488460..30807423hg38UCSC Ensembl
Innerchr15:30792569..31088477hg19UCSC Ensembl
Outerchr15:30780663..31099626hg19UCSC Ensembl
Innerchr15:28579861..28875769hg18UCSC Ensembl
Outerchr15:28567955..28886918hg18UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg38318964
hg19318964
hg18318964
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169498
Supporting Variants
SamplesNGO_30
Known GenesARHGAP11B, GOLGA8H, LOC100288637, ULK4P1, ULK4P2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244729
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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