A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6845



Internal ID15551795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:30321410..30366617hg38UCSC Ensembl
OuterchrX:30339527..30384734hg19UCSC Ensembl
OuterchrX:30249448..30294655hg18UCSC Ensembl
OuterchrX:30099184..30144391hg17UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3845208
hg1945208
hg1845208
hg1745208
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8701
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)nsv6845
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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