A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169920



Internal ID21313731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:119287958..119292266hg38UCSC Ensembl
Outerchr2:119287781..119293268hg38UCSC Ensembl
Innerchr2:120045534..120049842hg19UCSC Ensembl
Outerchr2:120045357..120050844hg19UCSC Ensembl
Innerchr2:119762004..119766312hg18UCSC Ensembl
Outerchr2:119761827..119767314hg18UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg385488
hg195488
hg185488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250069
SamplesNGO_20
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169920
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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