A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9777



Internal ID15193145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:55441203..55493280hg38UCSC Ensembl
OuterchrX:55467636..55519713hg19UCSC Ensembl
OuterchrX:55484361..55536438hg18UCSC Ensembl
OuterchrX:55350657..55402734hg17UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3852078
hg1952078
hg1852078
hg1752078
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7448
Supporting Variants
SamplesNA18507
Known GenesMAGEH1, MIR4536-1, USP51
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)nssv9777
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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