A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025321



Internal ID18767853
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106992302..107234753hg38UCSC Ensembl
Innerchr6:107313502..107555957hg19UCSC Ensembl
Innerchr6:107420195..107662650hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38242452
hg19242456
hg18242456
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6135n100
Supporting Variantsnssv3654282
Samples
Known GenesBEND3, C6orf203, PDSS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025321
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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