A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118239



Internal ID19277325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:51848316..51849216hg38UCSC Ensembl
Outerchr12:52242100..52243000hg19UCSC Ensembl
Cytoband12q13.13
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3980910
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118239
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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