A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126755



Internal ID18933212
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:113859824..113860424hg38UCSC Ensembl
Outerchr6:114181000..114181600hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985026
SamplesKWS1
Known GenesMARCKS
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126755
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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