A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019898



Internal ID18762433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:106988892..107233241hg38UCSC Ensembl
Innerchr6:107310094..107554445hg19UCSC Ensembl
Innerchr6:107416787..107661138hg18UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38244350
hg19244352
hg18244352
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6135n100
Supporting Variantsnssv3654280
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)nsv1019898
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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