A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244057



Internal ID21311503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:143764769..143928045hg38UCSC Ensembl
Outerchr1:143764768..143934634hg38UCSC Ensembl
Innerchr1:149259417..149422617hg19UCSC Ensembl
Outerchr1:149259416..149429206hg19UCSC Ensembl
Innerchr1:147526041..147689241hg18UCSC Ensembl
Outerchr1:147526040..147695830hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38169867
hg19169791
hg18169791
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169781
Supporting Variants
SamplesSNI_10
Known GenesFCGR1C, LOC388692
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244057
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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