A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170144



Internal ID21314205
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:93245637..93644800hg38UCSC Ensembl
Outerchr4:93238507..93647963hg38UCSC Ensembl
Innerchr4:94166788..94565951hg19UCSC Ensembl
Outerchr4:94159658..94569114hg19UCSC Ensembl
Innerchr4:94385811..94784974hg18UCSC Ensembl
Outerchr4:94378681..94788137hg18UCSC Ensembl
Cytoband4q22.2
Allele length
AssemblyAllele length
hg38409457
hg19409457
hg18409457
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242751
SamplesNGO_28
Known GenesGRID2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170144
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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