A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14246553



Internal ID21308044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:23872380..23877121hg38UCSC Ensembl
Outerchr10:23871573..23877853hg38UCSC Ensembl
Innerchr10:24161309..24166050hg19UCSC Ensembl
Outerchr10:24160502..24166782hg19UCSC Ensembl
Innerchr10:24201315..24206056hg18UCSC Ensembl
Outerchr10:24200508..24206788hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg386281
hg196281
hg186281
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170068
Supporting Variants
SamplesNGO_39
Known GenesKIAA1217
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14246553
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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