A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14251391



Internal ID21308597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:168804230..168821314hg38UCSC Ensembl
Outerchr4:168803875..168823416hg38UCSC Ensembl
Innerchr4:169725381..169742465hg19UCSC Ensembl
Outerchr4:169725026..169744567hg19UCSC Ensembl
Innerchr4:169961956..169979040hg18UCSC Ensembl
Outerchr4:169961601..169981142hg18UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg3819542
hg1919542
hg1819542
Variant TypeCNV deletion
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169825
Supporting Variants
SamplesNGO_43
Known GenesPALLD
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14251391
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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