A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135822



Internal ID18928071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88501164..88501294hg38UCSC Ensembl
Outerchr16:88567572..88567702hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38131
hg19131
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989413
SamplesKWS2
Known GenesZFPM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135822
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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