A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169824



Internal ID21313635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:13632829..13689865hg38UCSC Ensembl
Outerchr2:13631753..13691912hg38UCSC Ensembl
Innerchr2:13772954..13829990hg19UCSC Ensembl
Outerchr2:13771878..13832037hg19UCSC Ensembl
Innerchr2:13690405..13747441hg18UCSC Ensembl
Outerchr2:13689329..13749488hg18UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg3860160
hg1960160
hg1860160
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14248526
SamplesNGO_32
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169824
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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