A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025900



Internal ID18768432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106081902..106450546hg38UCSC Ensembl
Innerchr6:106529777..106898421hg19UCSC Ensembl
Innerchr6:106636470..107005114hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38368645
hg19368645
hg18368645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6134n100
Supporting Variantsnssv3654276
Samples
Known GenesATG5, PRDM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025900
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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