A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112712



Internal ID18909952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:49361638..49362738hg38UCSC Ensembl
Outerchr17:47439000..47440100hg19UCSC Ensembl
Cytoband17q21.33
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3967200
SamplesKWS2
Known GenesZNF652
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112712
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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