A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025014



Internal ID19114232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:124566073..124588709hg38UCSC Ensembl
Innerchr8:125578314..125600950hg19UCSC Ensembl
Innerchr8:125647495..125670131hg18UCSC Ensembl
Cytoband8q24.13
Allele length
AssemblyAllele length
hg3822637
hg1922637
hg1822637
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7309n100
Supporting Variantsnssv3691506
Samples
Known GenesMTSS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025014
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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