A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138553



Internal ID18901799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:49306909..49306973hg38UCSC Ensembl
Outerchr17:47384271..47384335hg19UCSC Ensembl
Cytoband17q21.32
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3972113, nssv3954569
SamplesKWS1, KWS2
Known GenesZNF652
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138553
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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