A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6849



Internal ID15551799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:31977200..32022281hg38UCSC Ensembl
OuterchrX:31995317..32040398hg19UCSC Ensembl
OuterchrX:31905238..31950319hg18UCSC Ensembl
OuterchrX:31754974..31800055hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg3845082
hg1945082
hg1845082
hg1745082
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8703
SamplesNA12156
Known GenesDMD
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)nsv6849
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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