A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013186



Internal ID19102404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:118462860..118506040hg38UCSC Ensembl
Innerchr1:119005483..119048663hg19UCSC Ensembl
Innerchr1:118807006..118850186hg18UCSC Ensembl
Cytoband1p12
Allele length
AssemblyAllele length
hg3843181
hg1943181
hg1843181
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3496934
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013186
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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