A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6956



Internal ID15205231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:71962628..72007933hg38UCSC Ensembl
OuterchrX:71182478..71227783hg19UCSC Ensembl
OuterchrX:71099203..71144508hg18UCSC Ensembl
OuterchrX:70965499..71010804hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3845306
hg1945306
hg1845306
hg1745306
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8741
SamplesNA12156
Known GenesNHSL2
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)nsv6956
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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