A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138485



Internal ID18911526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:89396958..89397023hg38UCSC Ensembl
Outerchr16:89463366..89463431hg19UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991059
SamplesKWS2
Known GenesANKRD11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138485
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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