A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127096



Internal ID18901035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:30451110..30451160hg38UCSC Ensembl
Outerchr10:30740039..30740089hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985437
SamplesKWS1
Known GenesMAP3K8
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127096
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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