A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8708



Internal ID15535156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:37931903..37954105hg38UCSC Ensembl
OuterchrX:37791156..37813358hg19UCSC Ensembl
OuterchrX:37676100..37698302hg18UCSC Ensembl
OuterchrX:37547373..37569575hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg3822203
hg1922203
hg1822203
hg1722203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6864
Supporting Variants
SamplesNA12156
Known Genes
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)nssv8708
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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