A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1151586



Internal ID18855329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:15229375..15229430hg38UCSC Ensembl
Outerchr10:15271374..15271429hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4003009
SamplesKWB1
Known GenesFAM171A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1151586
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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