A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6862



Internal ID15551814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:36886518..36919353hg38UCSC Ensembl
OuterchrX:36904591..36937426hg19UCSC Ensembl
OuterchrX:36814512..36847347hg18UCSC Ensembl
OuterchrX:36664248..36697083hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg388154
hg198154
hg188154
hg178154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv859
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)nsv6862
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