A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14249419



Internal ID21306378
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:188223152..189006348hg38UCSC Ensembl
Outerchr4:188222321..189009074hg38UCSC Ensembl
Innerchr4:189144306..189927502hg19UCSC Ensembl
Outerchr4:189143475..189930228hg19UCSC Ensembl
Innerchr4:189381300..190164496hg18UCSC Ensembl
Outerchr4:189380469..190167222hg18UCSC Ensembl
Cytoband4q35.2
Allele length
AssemblyAllele length
hg38786754
hg19786754
hg18786754
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169506
Supporting Variants
SamplesNGO_27
Known GenesLINC01060
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14249419
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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