A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999032



Internal ID18811882
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109644594..109700319hg38UCSC Ensembl
Innerchr1:110187216..110242941hg19UCSC Ensembl
Innerchr1:109988739..110044464hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3855726
hg1955726
hg1855726
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv254n100
Supporting Variantsnssv3494876, nssv3499755, nssv3485415, nssv3489386, nssv3488446, nssv3701155, nssv3701154
Samples
Known GenesGSTM1, GSTM2, GSTM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv999032
Frequency
Sample Size29084
Observed Gain4
Observed Loss3
Observed Complex0
Frequencyn/a


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