A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14244826



Internal ID21305951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:143764769..143942271hg38UCSC Ensembl
Outerchr1:143764768..144572337hg38UCSC Ensembl
Innerchr1:149259417..149436842hg19UCSC Ensembl
Outerchr1:149259416..149521840hg19UCSC Ensembl
Innerchr1:147526041..147703466hg18UCSC Ensembl
Outerchr1:147526040..147788464hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38807570
hg19262425
hg18262425
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3169781
Supporting Variants
SamplesNGO_24
Known GenesFCGR1C, LOC388692
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14244826
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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