A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6888



Internal ID15551842
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:47688074..47720852hg38UCSC Ensembl
OuterchrX:47547473..47580251hg19UCSC Ensembl
OuterchrX:47432417..47465195hg18UCSC Ensembl
OuterchrX:47303727..47336505hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg386628
hg196628
hg186628
hg176628
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6325
SamplesNA12156
Known GenesCXXC1P1
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)nsv6888
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