A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022069



Internal ID19111287
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:102022725..102150369hg38UCSC Ensembl
Innerchr6:102470600..102598244hg19UCSC Ensembl
Innerchr6:102577293..102704937hg18UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38127645
hg19127645
hg18127645
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3751265
Samples
Known GenesGRIK2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1022069
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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