A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025802



Internal ID19115019
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:11331518..11398845hg38UCSC Ensembl
Innerchr7:11371145..11438472hg19UCSC Ensembl
Innerchr7:11337670..11404997hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3867328
hg1967328
hg1867328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3642931
Samples
Known GenesTHSD7A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025802
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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