A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170201



Internal ID21314262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:189642489..189646849hg38UCSC Ensembl
Outerchr3:189642114..189653199hg38UCSC Ensembl
Innerchr3:189360278..189364638hg19UCSC Ensembl
Outerchr3:189359903..189370988hg19UCSC Ensembl
Innerchr3:190842972..190847332hg18UCSC Ensembl
Outerchr3:190842597..190853682hg18UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg3811086
hg1911086
hg1811086
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247591
SamplesSNI_4
Known GenesTP63
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170201
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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