A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1008797



Internal ID18751328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:18629403..18677739hg38UCSC Ensembl
Innerchr1:18955897..19004233hg19UCSC Ensembl
Innerchr1:18828484..18876820hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3848337
hg1948337
hg1848337
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3482266
Samples
Known GenesPAX7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1008797
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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