A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7463



Internal ID15552475
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:148349274..148389075hg38UCSC Ensembl
OuterchrX:147430794..147470595hg19UCSC Ensembl
OuterchrX:147238486..147278287hg18UCSC Ensembl
OuterchrX:147136340..147176141hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3839802
hg1939802
hg1839802
hg1739802
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6384
SamplesNA12156
Known Genes
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)nsv7463
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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