A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7153



Internal ID15552134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:151266389..151312191hg38UCSC Ensembl
OuterchrX:150434861..150480663hg19UCSC Ensembl
OuterchrX:150185519..150231321hg18UCSC Ensembl
OuterchrX:150105429..150151231hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3845803
hg1945803
hg1845803
hg1745803
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6388
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)nsv7153
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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