A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015920



Internal ID18758454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52758309..52797896hg38UCSC Ensembl
Innerchr6:52623107..52662694hg19UCSC Ensembl
Innerchr6:52731066..52770653hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3839588
hg1939588
hg1839588
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5962n100
Supporting Variantsnssv3657462, nssv3745488, nssv3657464, nssv3657465, nssv3657463
Samples
Known GenesGSTA1, GSTA2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015920
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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