A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034358



Internal ID18776892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26102760..26179939hg38UCSC Ensembl
Innerchr7:26142380..26219559hg19UCSC Ensembl
Innerchr7:26108905..26186084hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3877180
hg1977180
hg1877180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752934
Samples
Known GenesNFE2L3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034358
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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