A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988590



Internal ID19227153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:37418880..37422292hg38UCSC Ensembl
Outerchr17:35778964..35782398hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg383413
hg193435
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1135042
Supporting Variants
SamplesKWS2
Known GenesTADA2A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988590
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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