A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998086



Internal ID19157623
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 StatusM
Merged Variants
Supporting Variantsnssv3465849
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)nsv998086
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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