A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7029



Internal ID15205311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:107444874..107474624hg38UCSC Ensembl
OuterchrX:106688104..106717854hg19UCSC Ensembl
OuterchrX:106574760..106604510hg18UCSC Ensembl
OuterchrX:106494249..106523999hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg386024
hg196024
hg186024
hg176024
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5246
SamplesNA19129
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)nsv7029
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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