A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112285



Internal ID18930761
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:9774009..9774111hg38UCSC Ensembl
Outerchr16:9867866..9867968hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38103
hg19103
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3965984
SamplesKWS2
Known GenesGRIN2A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112285
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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