A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7119



Internal ID15552096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:140351842..140380600hg38UCSC Ensembl
OuterchrX:139434007..139462765hg19UCSC Ensembl
OuterchrX:139261673..139290431hg18UCSC Ensembl
OuterchrX:139159527..139188285hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3812236
hg1912236
hg1812236
hg1712236
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv919
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)nsv7119
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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