A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126240



Internal ID18928232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:3785108..3785708hg38UCSC Ensembl
Outerchr10:3827300..3827900hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984473
SamplesKWS1
Known GenesKLF6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126240
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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