A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3778



Internal ID15538506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:45648559..45691534hg38UCSC Ensembl
OuterchrX:45507804..45550779hg19UCSC Ensembl
OuterchrX:45392748..45435723hg18UCSC Ensembl
OuterchrX:45264058..45307033hg17UCSC Ensembl
CytobandXp11.3
Allele length
AssemblyAllele length
hg3842976
hg1942976
hg1842976
hg1742976
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7439
Supporting Variants
SamplesNA12878
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)nssv3778
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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