A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143872



Internal ID19280095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:83162131..83202731hg38UCSC Ensembl
Outerchr17:81109900..81150500hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3840601
hg1940601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1531n106
Supporting Variantsnssv3994569
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143872
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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