A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14242412



Internal ID21309514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42111518..42115486hg38UCSC Ensembl
Outerchr15:42110647..42120093hg38UCSC Ensembl
Innerchr15:42403716..42407684hg19UCSC Ensembl
Outerchr15:42402845..42412291hg19UCSC Ensembl
Innerchr15:40191008..40194976hg18UCSC Ensembl
Outerchr15:40190137..40199583hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg389447
hg199447
hg189447
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170209
Supporting Variants
SamplesNGO_50
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14242412
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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