A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169983



Internal ID21314044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:136595624..136699366hg38UCSC Ensembl
Outerchr4:136590928..136703669hg38UCSC Ensembl
Innerchr4:137516779..137620521hg19UCSC Ensembl
Outerchr4:137512083..137624824hg19UCSC Ensembl
Innerchr4:137736229..137839971hg18UCSC Ensembl
Outerchr4:137731533..137844274hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38112742
hg19112742
hg18112742
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245703, nssv14241184
SamplesNGO_12, MLY_11
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169983
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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