A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6860



Internal ID15551812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:35002580..35051491hg38UCSC Ensembl
OuterchrX:35020697..35069608hg19UCSC Ensembl
OuterchrX:34930618..34979529hg18UCSC Ensembl
OuterchrX:34780354..34829265hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg387066
hg197066
hg187066
hg177066
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6320, nssv858
SamplesNA12156, NA19240
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)nsv6860
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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