A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10706



Internal ID15195406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:49328477..49330226hg38UCSC Ensembl
OuterchrX:49184957..49186704hg19UCSC Ensembl
OuterchrX:49071901..49073648hg18UCSC Ensembl
OuterchrX:48941328..48943075hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3836350
hg1936350
hg1836350
hg1736350
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6897
Supporting Variants
SamplesNA18956
Known GenesGAGE12J
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)nssv10706
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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