A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024654



Internal ID18767186
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167249012..167405373hg38UCSC Ensembl
Innerchr6:167662500..167818861hg19UCSC Ensembl
Innerchr6:167582490..167738851hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg38156362
hg19156362
hg18156362
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655418
Samples
Known GenesTCP10, TTLL2, UNC93A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024654
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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