A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169506



Internal ID21313739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188221875..189006348hg38UCSC Ensembl
Outerchr4:188218104..189009074hg38UCSC Ensembl
Innerchr4:189143029..189927502hg19UCSC Ensembl
Outerchr4:189139258..189930228hg19UCSC Ensembl
Innerchr4:189380023..190164496hg18UCSC Ensembl
Outerchr4:189376252..190167222hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38790971
hg19790971
hg18790971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14244296, nssv14249419
SamplesNGO_27, SNI_16
Known GenesLINC01060
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169506
Frequency
Sample Size93
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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