A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3973117



Internal ID19238537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:51507851..51507914hg38UCSC Ensembl
Outerchr3:51541867..51541930hg19UCSC Ensembl
Cytoband3p21.2
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1136724
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3973117
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