A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1123693



Internal ID19277576
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:136538897..136538952hg38UCSC Ensembl
Outerchr3:136257739..136257794hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3973466
SamplesKWS2
Known GenesSTAG1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1123693
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