A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981056



Internal ID19209037
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:17681286..17682286hg38UCSC Ensembl
Outerchr17:17584600..17585600hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118747
Supporting Variants
SamplesKWS1
Known GenesRAI1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981056
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