A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3467117



Internal ID18715450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:17277110..17368206hg38UCSC Ensembl
Innerchr1:17603605..17694701hg19UCSC Ensembl
Innerchr1:17476192..17567288hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3891097
hg1991097
hg1891097
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1003937
Supporting Variants
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)nssv3467117
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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