A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244878



Internal ID21303949
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76048529..76052548hg38UCSC Ensembl
Outerchr15:76042215..76056133hg38UCSC Ensembl
Innerchr15:76340870..76344889hg19UCSC Ensembl
Outerchr15:76334556..76348474hg19UCSC Ensembl
Innerchr15:74127925..74131944hg18UCSC Ensembl
Outerchr15:74121611..74135529hg18UCSC Ensembl
Cytoband15q24.2
Allele length
AssemblyAllele length
hg3813919
hg1913919
hg1813919
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169600
Supporting Variants
SamplesNGO_1
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244878
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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