A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4000382



Internal ID18840895
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 StatusS
Merged Variantsnsv1148344
Supporting Variants
SamplesKWB1
Known GenesZFPM1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4000382
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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