A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6807



Internal ID15551753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:14260884..14296900hg38UCSC Ensembl
OuterchrX:14279006..14315022hg19UCSC Ensembl
OuterchrX:14188927..14224943hg18UCSC Ensembl
OuterchrX:14038663..14074679hg17UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg3836017
hg1936017
hg1836017
hg1736017
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8688
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)nsv6807
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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