A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113251



Internal ID19279913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:11197000..11197083hg38UCSC Ensembl
Outerchr10:11238963..11239046hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3968158
SamplesKWS2
Known GenesCELF2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113251
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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