A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7006



Internal ID15551972
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:99164642..99232555hg38UCSC Ensembl
OuterchrX:98419640..98487553hg19UCSC Ensembl
OuterchrX:98306296..98374209hg18UCSC Ensembl
OuterchrX:98225785..98293698hg17UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg3867914
hg1967914
hg1867914
hg1767914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8753, nssv5241
SamplesNA12156, NA19129
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)nsv7006
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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