A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143852



Internal ID18903482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:36180924..36242254hg38UCSC Ensembl
Outerchr17:34508300..34569700hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3861331
hg1961401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994548
SamplesKWS1
Known GenesCCL3L1, CCL3L3, CCL4L1, CCL4L2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143852
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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