A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1152166



Internal ID18856020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:139326279..139329349hg38UCSC Ensembl
Outerchr5:138661968..138665038hg19UCSC Ensembl
Cytoband5q31.2
Allele length
AssemblyAllele length
hg383071
hg193071
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3996773
SamplesKWB1
Known GenesMATR3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1152166
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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