A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1004059



Internal ID19093276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109683331..109700319hg38UCSC Ensembl
Innerchr1:110225953..110242941hg19UCSC Ensembl
Innerchr1:110027476..110044464hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3816989
hg1916989
hg1816989
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv268n100
Supporting Variantsnssv3501013, nssv3488386, nssv3494558, nssv3487256, nssv3494889, nssv3499772, nssv3494391
Samples
Known GenesGSTM1, GSTM2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1004059
Frequency
Sample Size11257
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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