A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999034



Internal ID17291986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:22554596..22565595hg38UCSC Ensembl
Outerchr15:23307501..23318500hg19UCSC Ensembl
Cytoband15q11.2
Allele length
AssemblyAllele length
hg3811000
hg1911000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952567
Supporting Variants
SamplesBILGI_BIOE
Known GenesHERC2P2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999034
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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