A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14247632



Internal ID21303678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:76598900..76603434hg38UCSC Ensembl
Outerchr15:76586021..76609838hg38UCSC Ensembl
Innerchr15:76891241..76895775hg19UCSC Ensembl
Outerchr15:76878362..76902179hg19UCSC Ensembl
Innerchr15:74678296..74682830hg18UCSC Ensembl
Outerchr15:74665417..74689234hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg3823818
hg1923818
hg1823818
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170280
Supporting Variants
SamplesMLY_8
Known GenesSCAPER
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14247632
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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