A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138411



Internal ID18938236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:8564477..8564601hg38UCSC Ensembl
Outerchr16:8614479..8614603hg19UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990980, nssv3954793
SamplesKWS1, KWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138411
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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