A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122494



Internal ID18923467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13713800..13713859hg38UCSC Ensembl
Outerchr10:13755800..13755859hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970696
SamplesKWS2
Known GenesFRMD4A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122494
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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