A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143641



Internal ID18902507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:45876167..45959243hg38UCSC Ensembl
Outerchr10:51636600..51722700hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3883077
hg1986101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv454n106
Supporting Variantsnssv3994327
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143641
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