A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952596



Internal ID16954783
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:30392098..30407197hg38UCSC Ensembl
Outerchr15:30684301..30699400hg19UCSC Ensembl
Cytoband15q13.2
Allele length
AssemblyAllele length
hg3815100
hg1915100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999063
SamplesBILGI_BIOE
Known GenesCHRFAM7A, LOC101059918
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952596
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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