A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3990909



Internal ID19235856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:28140997..28141059hg38UCSC Ensembl
Outerchr15:28386143..28386205hg19UCSC Ensembl
Cytoband15q13.1
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113697
Supporting Variants
SamplesKWS2
Known GenesHERC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3990909
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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