A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv998403



Internal ID19157939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:98241337..98339345hg38UCSC Ensembl
Innerchr1:98706893..98804901hg19UCSC Ensembl
Innerchr1:98479481..98577489hg18UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg3898009
hg1998009
hg1898009
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3699603
Samples
Known GenesLOC729987
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv998403
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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