A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144777



Internal ID18927312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:85613594..85614494hg38UCSC Ensembl
Outerchr16:85647200..85648100hg19UCSC Ensembl
Cytoband16q24.1
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981369
SamplesKWS1
Known GenesGSE1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144777
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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