A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026390



Internal ID19115608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:64779945..64953986hg38UCSC Ensembl
Innerchr7:64240323..64414364hg19UCSC Ensembl
Innerchr7:63877758..64051799hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38174042
hg19174042
hg18174042
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655505
Samples
Known GenesZNF138, ZNF273
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026390
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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