A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1001905



Internal ID19091122
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:79944778..79993645hg38UCSC Ensembl
Innerchr1:80410463..80459330hg19UCSC Ensembl
Innerchr1:80183051..80231918hg18UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3848868
hg1948868
hg1848868
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3463185
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)nsv1001905
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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