A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013520



Internal ID19102738
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9266587..9344909hg38UCSC Ensembl
Innerchr1:9326646..9404968hg19UCSC Ensembl
Innerchr1:9249233..9327555hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3878323
hg1978323
hg1878323
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv17n100
Supporting Variantsnssv3477770, nssv3462890, nssv3473608, nssv3480223, nssv3482473
Samples
Known GenesH6PD, SPSB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1013520
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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