A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020575



Internal ID18763110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52754424..52767793hg38UCSC Ensembl
Innerchr6:52619222..52632591hg19UCSC Ensembl
Innerchr6:52727181..52740550hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3813370
hg1913370
hg1813370
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3745486
Samples
Known GenesGSTA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020575
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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