A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1121339



Internal ID18925892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:666376..667821hg38UCSC Ensembl
Outerchr6:666376..667821hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg381446
hg191446
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3248n106
Supporting Variantsnssv3965811, nssv3972100
SamplesKWS2, KWS1
Known GenesEXOC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1121339
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