A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170068



Internal ID21314129
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14240991, nssv14246553
SamplesNGO_39, NGO_49
Known GenesKIAA1217
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170068
Frequency
Sample Size93
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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