A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169472



Internal ID21313955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:64377044..64385862hg38UCSC Ensembl
Outerchr1:64371598..64388922hg38UCSC Ensembl
Innerchr1:64842727..64851545hg19UCSC Ensembl
Outerchr1:64837281..64854605hg19UCSC Ensembl
Innerchr1:64615315..64624133hg18UCSC Ensembl
Outerchr1:64609869..64627193hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3817325
hg1917325
hg1817325
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14250894, nssv14247796
SamplesNGO_1, MLY_10
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169472
Frequency
Sample Size93
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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