A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6391



Internal ID15537472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:155559920..155582713hg38UCSC Ensembl
OuterchrX:154789581..154812374hg19UCSC Ensembl
OuterchrX:154442775..154465568hg18UCSC Ensembl
OuterchrX:154353285..154376078hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3822794
hg1922794
hg1822794
hg1722794
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7162
Supporting Variants
SamplesNA12156
Known GenesTMLHE
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)nssv6391
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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