A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14248317



Internal ID21308614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:8253504..8270494hg38UCSC Ensembl
Outerchr10:8251303..8277131hg38UCSC Ensembl
Innerchr10:8295467..8312457hg19UCSC Ensembl
Outerchr10:8293266..8319094hg19UCSC Ensembl
Innerchr10:8335473..8352463hg18UCSC Ensembl
Outerchr10:8333272..8359100hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3825829
hg1925829
hg1825829
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169999
Supporting Variants
SamplesNGO_43
Known GenesLINC00708
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14248317
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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