A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024657



Internal ID18767189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167112710..167142000hg38UCSC Ensembl
Innerchr6:167526198..167555488hg19UCSC Ensembl
Innerchr6:167446188..167475478hg18UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3829291
hg1929291
hg1829291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749621
Samples
Known GenesCCR6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024657
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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