A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138568



Internal ID19272549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:67269191..67269246hg38UCSC Ensembl
Outerchr17:65265307..65265362hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991157
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138568
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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