A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968929



Internal ID19246603
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:111322288..111322356hg38UCSC Ensembl
Outerchr13:111974635..111974703hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113609
Supporting Variants
SamplesKWS2
Known GenesTEX29
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968929
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