A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6885



Internal ID15551839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:46648550..46693561hg38UCSC Ensembl
OuterchrX:46507985..46552996hg19UCSC Ensembl
OuterchrX:46392929..46437940hg18UCSC Ensembl
OuterchrX:46264239..46309250hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3845012
hg1945012
hg1845012
hg1745012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8717
SamplesNA12156
Known GenesSLC9A7
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)nsv6885
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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