A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv885



Internal ID15545104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:72994850..73045938hg38UCSC Ensembl
OuterchrX:72214689..72265777hg19UCSC Ensembl
OuterchrX:72131414..72182502hg18UCSC Ensembl
OuterchrX:71997710..72048798hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3851089
hg1951089
hg1851089
hg1751089
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7451
Supporting Variants
SamplesNA19240
Known GenesPABPC1L2B
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)nssv885
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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