A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170151



Internal ID21314212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:119287244..119319784hg38UCSC Ensembl
Outerchr6:119280939..119319888hg38UCSC Ensembl
Innerchr6:119608409..119640949hg19UCSC Ensembl
Outerchr6:119602104..119641053hg19UCSC Ensembl
Innerchr6:119650108..119682648hg18UCSC Ensembl
Outerchr6:119643803..119682752hg18UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg3838950
hg1938950
hg1838950
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244031
SamplesNGO_32
Known GenesMAN1A1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170151
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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