A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1011098



Internal ID18753632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17251870..17309505hg38UCSC Ensembl
Innerchr1:17578365..17636000hg19UCSC Ensembl
Innerchr1:17450952..17508587hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3857636
hg1957636
hg1857636
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv128n100
Supporting Variantsnssv3471098
Samples
Known GenesPADI3, PADI4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1011098
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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