A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8712



Internal ID15535152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:41025030..41033866hg38UCSC Ensembl
OuterchrX:40884283..40893119hg19UCSC Ensembl
OuterchrX:40769227..40778063hg18UCSC Ensembl
OuterchrX:40640537..40649373hg17UCSC Ensembl
CytobandXp11.4
Allele length
AssemblyAllele length
hg388837
hg198837
hg188837
hg178837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6873
Supporting Variants
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)nssv8712
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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