A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3465849



Internal ID19061439
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:101014144..101178642hg38UCSC Ensembl
Innerchr1:101479700..101644198hg19UCSC Ensembl
Innerchr1:101252288..101416786hg18UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg38164499
hg19164499
hg18164499
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv998086
Supporting Variants
Samples
Known GenesDPH5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3465849
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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