A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010486



Internal ID18753017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:206876486..207031685hg38UCSC Ensembl
Innerchr1:207049831..207205030hg19UCSC Ensembl
Innerchr1:205116454..205271653hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg38155200
hg19155200
hg18155200
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3705498
Samples
Known GenesC1orf116, FAIM3, FCAMR, IL24, PIGR
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010486
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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