A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124398



Internal ID18911790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:14568483..14568548hg38UCSC Ensembl
Outerchr10:14610482..14610547hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975693
SamplesKWS1
Known GenesFAM107B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124398
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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