A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6832



Internal ID15205095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:21900195..21946092hg38UCSC Ensembl
OuterchrX:21918313..21964210hg19UCSC Ensembl
OuterchrX:21828234..21874131hg18UCSC Ensembl
OuterchrX:21677970..21723867hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3845898
hg1945898
hg1845898
hg1745898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6316
SamplesNA12156
Known GenesSMS
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)nsv6832
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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