A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv723095



Internal ID15670365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:143538619..143949533hg38UCSC Ensembl
Innerchr1:149005557..149444104hg19UCSC Ensembl
Innerchr1:147272181..147710728hg18UCSC Ensembl
Cytoband1q21.1
Allele length
AssemblyAllele length
hg38410915
hg19438548
hg18438548
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv547687
Supporting Variants
Samples
Known GenesFCGR1C, LOC101929780, LOC388692, NBPF23
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv723095
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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