A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170079



Internal ID21314140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:53204794..53214075hg38UCSC Ensembl
Outerchr4:53200838..53220572hg38UCSC Ensembl
Innerchr4:54070961..54080242hg19UCSC Ensembl
Outerchr4:54067005..54086739hg19UCSC Ensembl
Innerchr4:53765718..53774999hg18UCSC Ensembl
Outerchr4:53761762..53781496hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3819735
hg1919735
hg1819735
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249767, nssv14251531
SamplesNGO_39, MLY_3
Known GenesSCFD2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170079
Frequency
Sample Size93
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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