A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7008



Internal ID15551974
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:100486135..100494524hg38UCSC Ensembl
OuterchrX:99741133..99749521hg19UCSC Ensembl
OuterchrX:99627789..99636177hg18UCSC Ensembl
OuterchrX:99547278..99555666hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg388390
hg198389
hg188389
hg178389
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8755
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)nsv7008
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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