A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977862



Internal ID18266381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:37014268..37017282hg38UCSC Ensembl
Innerchr15:37306469..37309483hg19UCSC Ensembl
Innerchr15:35093761..35096775hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg383015
hg193015
hg183015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2762261
SamplesHGDP01284
Known GenesMEIS2
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977862
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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