A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028720



Internal ID18771251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:52758710..52797896hg38UCSC Ensembl
Innerchr6:52623508..52662694hg19UCSC Ensembl
Innerchr6:52731467..52770653hg18UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3839187
hg1939187
hg1839187
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5962n100
Supporting Variantsnssv3657466, nssv3657467, nssv3745490
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)nsv1028720
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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