A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126441



Internal ID18904127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89618792..89619892hg38UCSC Ensembl
Outerchr16:89685200..89686300hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1388n106
Supporting Variantsnssv3984689
SamplesKWS1
Known GenesDPEP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126441
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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