A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009914



Internal ID18752445
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:9237601..9340463hg38UCSC Ensembl
Innerchr1:9297660..9400522hg19UCSC Ensembl
Innerchr1:9220247..9323109hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38102863
hg19102863
hg18102863
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv16n100
Supporting Variantsnssv3696767
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)nsv1009914
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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