A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6336



Internal ID15537527
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:56758738..56803766hg38UCSC Ensembl
OuterchrX:56785171..56830199hg19UCSC Ensembl
OuterchrX:56801896..56846924hg18UCSC Ensembl
OuterchrX:56668192..56713220hg17UCSC Ensembl
CytobandXp11.1
Allele length
AssemblyAllele length
hg3845029
hg1945029
hg1845029
hg1745029
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6917
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)nssv6336
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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