A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1010810



Internal ID19100027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:109690459..109707602hg38UCSC Ensembl
Innerchr1:110233081..110250224hg19UCSC Ensembl
Innerchr1:110034604..110051747hg18UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3817144
hg1917144
hg1817144
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv275n100
Supporting Variantsnssv3482917, nssv3494565
Samples
Known GenesGSTM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1010810
Frequency
Sample Size11257
Observed Gain1
Observed Loss1
Observed Complex0
Frequencyn/a


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