A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7061



Internal ID15205347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:120868676..120996041hg38UCSC Ensembl
OuterchrX:120002530..120129895hg19UCSC Ensembl
OuterchrX:119886558..119957576hg18UCSC Ensembl
OuterchrX:119784412..119855430hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38127366
hg19127366
hg1871019
hg1771019
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10734, nssv9252, nssv907, nssv1861, nssv5258, nssv9782, nssv6368
SamplesNA18507, NA12156, NA18956, NA18555, NA18517, NA19240, NA19129
Known GenesCT47A1, CT47A10, CT47A11, CT47A12, CT47A2, CT47A3, CT47A4, CT47A5, CT47A6, CT47A7, CT47A8, CT47A9, CT47B1
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)nsv7061
Frequency
Sample Size9
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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