A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136737



Internal ID19249572
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:72303263..72303313hg38UCSC Ensembl
Outerchr3:72352414..72352464hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg3851
hg1951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3986215, nssv3973430
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136737
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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