A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772436



Internal ID18960376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:10743282..10746683hg38UCSC Ensembl
chr17:10646599..10650000hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg383402
hg193402
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070808
Supporting Variants
SamplesKWP1
Known GenesTMEM220-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772436
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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