A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6905



Internal ID15551861
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:50966285..51006025hg38UCSC Ensembl
OuterchrX:50709285..50749025hg19UCSC Ensembl
OuterchrX:50726025..50765765hg18UCSC Ensembl
OuterchrX:50542321..50582061hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3839741
hg1939741
hg1839741
hg1739741
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8723
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)nsv6905
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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