A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1013944



Internal ID18756476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9247978..9351410hg38UCSC Ensembl
Innerchr1:9308037..9411469hg19UCSC Ensembl
Innerchr1:9230624..9334056hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38103433
hg19103433
hg18103433
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv16n100
Supporting Variantsnssv3477914
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)nsv1013944
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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