A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145454



Internal ID18937707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:49649881..49649946hg38UCSC Ensembl
Outerchr10:50857927..50857992hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982602
SamplesKWS1
Known GenesCHAT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145454
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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