A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251125



Internal ID21308132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:12791219..12795017hg38UCSC Ensembl
Outerchr8:12788880..12796024hg38UCSC Ensembl
Innerchr8:12648728..12652526hg19UCSC Ensembl
Outerchr8:12646389..12653533hg19UCSC Ensembl
Innerchr8:12693099..12696897hg18UCSC Ensembl
Outerchr8:12690760..12697904hg18UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg387145
hg197145
hg187145
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169625
Supporting Variants
SamplesNGO_4
Known GenesLINC00681, LOC340357
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251125
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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