A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv961754



Internal ID18597000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:68087758..68090922hg38UCSC Ensembl
Innerchr2:68314890..68318054hg19UCSC Ensembl
Innerchr2:68168394..68171558hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg383165
hg193165
hg183165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2764370
SamplesHGDP01029
Known Genes
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv961754
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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