A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952610



Internal ID16954797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:37094000..37102499hg38UCSC Ensembl
Outerchr15:37386201..37394700hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg388500
hg198500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999077
SamplesBILGI_BIOE
Known GenesMEIS2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952610
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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