A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121814



Internal ID18916816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:45876167..45959936hg38UCSC Ensembl
Outerchr10:51635900..51720700hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3883770
hg1984801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv454n106
Supporting Variantsnssv3968463
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121814
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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