A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9776



Internal ID15193144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:46971278..47003023hg38UCSC Ensembl
OuterchrX:46820935..46862425hg19UCSC Ensembl
OuterchrX:46705879..46747369hg18UCSC Ensembl
OuterchrX:46577189..46618679hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3831746
hg1941491
hg1841491
hg1741491
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7440
Supporting Variants
SamplesNA18507
Known GenesJADE3
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)nssv9776
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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