A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034981



Internal ID19124200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:91570352..91821130hg38UCSC Ensembl
Innerchr6:92280070..92530848hg19UCSC Ensembl
Innerchr6:92336791..92587569hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg38250779
hg19250779
hg18250779
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3751233
Samples
Known GenesCASC6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034981
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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