A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006916



Internal ID19096134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:4937443..4952295hg38UCSC Ensembl
Innerchr1:4997503..5012355hg19UCSC Ensembl
Innerchr1:4897363..4912215hg18UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3814853
hg1914853
hg1814853
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv14n100
Supporting Variantsnssv3474009
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)nsv1006916
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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