A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955338



Internal ID18874277
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:68552654..68552985hg38UCSC Ensembl
Outerchr17:66548795..66549126hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38332
hg19332
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127594
Supporting Variants
SamplesKWS1
Known GenesFAM20A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955338
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer