A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169830



Internal ID21313641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:72499576..72535253hg38UCSC Ensembl
Outerchr1:72498429..72537400hg38UCSC Ensembl
Innerchr1:72965259..73000936hg19UCSC Ensembl
Outerchr1:72964112..73003083hg19UCSC Ensembl
Innerchr1:72737847..72773524hg18UCSC Ensembl
Outerchr1:72736700..72775671hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3838972
hg1938972
hg1838972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250075
SamplesMLY_14
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169830
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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