A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6822



Internal ID15551770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:18850554..18885278hg38UCSC Ensembl
OuterchrX:18868672..18903396hg19UCSC Ensembl
OuterchrX:18778593..18813317hg18UCSC Ensembl
OuterchrX:18628329..18663053hg17UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg386274
hg196274
hg186274
hg176274
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv854
SamplesNA19240
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv6822
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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