A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127089



Internal ID18902417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:13094320..13094382hg38UCSC Ensembl
Outerchr10:13136320..13136382hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985426
SamplesKWS1
Known GenesCCDC3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127089
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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