A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6917



Internal ID15551874
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 Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6336, nssv3791
SamplesNA12156, NA12878
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)nsv6917
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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