A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6778



Internal ID15551721
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:3116993..3161877hg38UCSC Ensembl
OuterchrX:3035034..3079918hg19UCSC Ensembl
OuterchrX:3045034..3089918hg18UCSC Ensembl
OuterchrX:3028395..3073279hg17UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3844885
hg1944885
hg1844885
hg1744885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8679
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)nsv6778
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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