A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020107



Internal ID18762643
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:88129212..88157029hg38UCSC Ensembl
Innerchr6:88838931..88866748hg19UCSC Ensembl
Innerchr6:88895650..88923467hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3827818
hg1927818
hg1827818
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6086n100
Supporting Variantsnssv3648943
Samples
Known GenesCNR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020107
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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