A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6827



Internal ID15205089
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:20072602..20095381hg38UCSC Ensembl
OuterchrX:20090720..20113499hg19UCSC Ensembl
OuterchrX:20000641..20023420hg18UCSC Ensembl
OuterchrX:19850377..19873156hg17UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3822780
hg1922780
hg1822780
hg1722780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8697
SamplesNA12156
Known GenesMAP7D2
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)nsv6827
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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