A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169654



Internal ID21313465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:57185482..57234405hg38UCSC Ensembl
Outerchr4:57183027..57236258hg38UCSC Ensembl
Innerchr4:58051648..58100571hg19UCSC Ensembl
Outerchr4:58049193..58102424hg19UCSC Ensembl
Innerchr4:57746405..57795328hg18UCSC Ensembl
Outerchr4:57743950..57797181hg18UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3853232
hg1953232
hg1853232
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14247658
SamplesMLY_3
Known GenesIGFBP7-AS1
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169654
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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