A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1148344



Internal ID18849088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:88493107..88493214hg38UCSC Ensembl
Outerchr16:88559515..88559622hg19UCSC Ensembl
Cytoband16q24.2
Allele length
AssemblyAllele length
hg38108
hg19108
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4000382
SamplesKWB1
Known GenesZFPM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1148344
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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