A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133405



Internal ID18905221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:36177240..36223356hg38UCSC Ensembl
Outerchr17:34504600..34550800hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3846117
hg1946201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967840
SamplesKWS2
Known GenesCCL3L1, CCL3L3, CCL4L1, CCL4L2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133405
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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