A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124987



Internal ID19265880
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:156982006..156984206hg38UCSC Ensembl
Outerchr7:156774700..156776900hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg382201
hg192201
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3721n106
Supporting Variantsnssv3977793
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124987
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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