A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024624



Internal ID19113841
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162845669..162989670hg38UCSC Ensembl
Innerchr6:163266701..163410702hg19UCSC Ensembl
Innerchr6:163186691..163330692hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg38144002
hg19144002
hg18144002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749611
Samples
Known GenesPACRG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024624
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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