A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7118



Internal ID15205409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:140020153..140055396hg38UCSC Ensembl
OuterchrX:139102312..139137555hg19UCSC Ensembl
OuterchrX:138929978..138965221hg18UCSC Ensembl
OuterchrX:138827832..138863075hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg385749
hg195749
hg185749
hg175749
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv918
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)nsv7118
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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