A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6337



Internal ID15537526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:56772689..56787522hg38UCSC Ensembl
OuterchrX:56799122..56813955hg19UCSC Ensembl
OuterchrX:56815847..56830680hg18UCSC Ensembl
OuterchrX:56682143..56696976hg17UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg3814068
hg1914068
hg1814068
hg1714068
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6918
Supporting Variants
SamplesNA12156
Known GenesLOC550643
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)nssv6337
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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