A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169903



Internal ID21313714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:99393381..99556305hg38UCSC Ensembl
Outerchr4:99387827..99561532hg38UCSC Ensembl
Innerchr4:100314538..100477462hg19UCSC Ensembl
Outerchr4:100308984..100482689hg19UCSC Ensembl
Innerchr4:100533561..100696485hg18UCSC Ensembl
Outerchr4:100528007..100701712hg18UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg38173706
hg19173706
hg18173706
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244002, nssv14245113, nssv14245262, nssv14252177
SamplesNGO_41, NGO_30, NGO_20, NGO_44
Known GenesADH7, C4orf17, TRMT10A
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169903
Frequency
Sample Size93
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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