A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7056



Internal ID15552027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:119739370..119781029hg38UCSC Ensembl
OuterchrX:118873333..118914992hg19UCSC Ensembl
OuterchrX:118757361..118799020hg18UCSC Ensembl
OuterchrX:118655215..118696874hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3841660
hg1941660
hg1841660
hg1741660
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6367
SamplesNA12156
Known GenesSOWAHD
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)nsv7056
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer