A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524931



Internal ID15105538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:140958435..141130292hg38UCSC Ensembl
InnerchrX:140040600..140224480hg19UCSC Ensembl
InnerchrX:139868266..140052146hg18UCSC Ensembl
InnerchrX:139766120..139950000hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38171858
hg19183881
hg18183881
hg17183881
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700944
Samples
Known GenesSPANXB1, SPANXB2, SPANXF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524931
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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