A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6883



Internal ID15205151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:45865344..45884684hg38UCSC Ensembl
OuterchrX:45724779..45744119hg19UCSC Ensembl
OuterchrX:45609723..45629063hg18UCSC Ensembl
OuterchrX:45481033..45500373hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg387094
hg197094
hg187094
hg177094
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8716
SamplesNA12156
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)nsv6883
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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