A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124146



Internal ID19268471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:164012510..164012574hg38UCSC Ensembl
Outerchr6:164433542..164433606hg19UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975459
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124146
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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