A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1007097



Internal ID18749628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:151860320..152255501hg38UCSC Ensembl
Innerchr1:151832796..152227977hg19UCSC Ensembl
Innerchr1:150099420..150494601hg18UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38395182
hg19395182
hg18395182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3705033
Samples
Known GenesHRNR, NBPF18P, RPTN, S100A10, S100A11, TCHH, TCHHL1, THEM4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1007097
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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