A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6914



Internal ID15551871
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:55669111..55704923hg38UCSC Ensembl
OuterchrX:55695544..55731356hg19UCSC Ensembl
OuterchrX:55712269..55748081hg18UCSC Ensembl
OuterchrX:55578565..55614377hg17UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3835813
hg1935813
hg1835813
hg1735813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10714, nssv875
SamplesNA18956, NA19240
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)nsv6914
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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