A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027534



Internal ID18770066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:12857816..12877365hg38UCSC Ensembl
Innerchr6:12858048..12877597hg19UCSC Ensembl
Innerchr6:12966034..12985583hg18UCSC Ensembl
Cytoband6p24.1
Allele length
AssemblyAllele length
hg3819550
hg1919550
hg1819550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3749031
Samples
Known GenesPHACTR1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027534
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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