A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137123



Internal ID18936221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:87602912..87602968hg38UCSC Ensembl
Outerchr6:88312630..88312686hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975812
SamplesKWS2
Known GenesORC3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137123
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