A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3969580



Internal ID18889367
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:138692463..138693563hg38UCSC Ensembl
Outerchr6:139013600..139014700hg19UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg381101
hg191101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1122139
Supporting Variants
SamplesKWS2
Known GenesFLJ46906
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3969580
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