A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143832



Internal ID18929900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88533492..88534692hg38UCSC Ensembl
Outerchr16:88599900..88601100hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994528
SamplesKWS1
Known GenesZFPM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143832
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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