A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv684706



Internal ID15421358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:70651742..70727834hg38UCSC Ensembl
InnerchrX:69871592..69947684hg19UCSC Ensembl
InnerchrX:69788317..69864409hg18UCSC Ensembl
InnerchrX:69654613..69730705hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3876093
hg1976093
hg1876093
hg1776093
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517078
Supporting Variants
Samples
Known GenesTEX11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv684706
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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