A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677046



Internal ID15067012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141136956..141608987hg38UCSC Ensembl
InnerchrX:140231141..140697115hg19UCSC Ensembl
InnerchrX:140058807..140524781hg18UCSC Ensembl
InnerchrX:139956661..140422635hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38472032
hg19465975
hg18465975
hg17465975
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516880
Supporting Variants
Samples
Known GenesLDOC1, SPANXA1, SPANXA2, SPANXA2-OT1, SPANXC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677046
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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