A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023549



Internal ID18766082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:88132826..88159329hg38UCSC Ensembl
Innerchr6:88842545..88869048hg19UCSC Ensembl
Innerchr6:88899264..88925767hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3826504
hg1926504
hg1826504
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6086n100
Supporting Variantsnssv3750122
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)nsv1023549
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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