A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6906



Internal ID15205176
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:51806291..51850971hg38UCSC Ensembl
OuterchrX:51549387..51594067hg19UCSC Ensembl
OuterchrX:51566127..51610807hg18UCSC Ensembl
OuterchrX:51382423..51427103hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3844681
hg1944681
hg1844681
hg1744681
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8724
SamplesNA12156
Known GenesMAGED1
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)nsv6906
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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