A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009355



Internal ID18751886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:45723586..45997340hg38UCSC Ensembl
Innerchr1:46189258..46463012hg19UCSC Ensembl
Innerchr1:45961845..46235599hg18UCSC Ensembl
Cytoband1p34.1
Allele length
AssemblyAllele length
hg38273755
hg19273755
hg18273755
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv159n100
Supporting Variantsnssv3467512
Samples
Known GenesIPP, MAST2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009355
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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