A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7037



Internal ID15205320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:110684665..110729447hg38UCSC Ensembl
OuterchrX:109927893..109972675hg19UCSC Ensembl
OuterchrX:109814549..109859331hg18UCSC Ensembl
OuterchrX:109734038..109778820hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3844783
hg1944783
hg1844783
hg1744783
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5247
SamplesNA19129
Known GenesCHRDL1
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)nsv7037
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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