A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021849



Internal ID18764383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:149533838..149725148hg38UCSC Ensembl
Innerchr7:149230929..149422239hg19UCSC Ensembl
Innerchr7:148861862..149053172hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38191311
hg19191311
hg18191311
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674238
Samples
Known GenesKRBA1, ZNF767
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1021849
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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