A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2762261



Internal ID17528780
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 Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv977862
Supporting Variants
SamplesHGDP01284
Known GenesMEIS2
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2762261
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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