A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6331



Internal ID15537532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:52906461..52992080hg38UCSC Ensembl
OuterchrX:52935488..53021260hg19UCSC Ensembl
OuterchrX:52952213..53037985hg18UCSC Ensembl
OuterchrX:52818509..52904281hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3885620
hg1985773
hg1885773
hg1785773
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7447
Supporting Variants
SamplesNA12156
Known GenesFAM156A, FAM156B
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)nssv6331
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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