A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672692



Internal ID15062658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141221989..141667150hg38UCSC Ensembl
InnerchrX:140316168..140755302hg19UCSC Ensembl
InnerchrX:140143834..140582968hg18UCSC Ensembl
InnerchrX:140041688..140480822hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38445162
hg19439135
hg18439135
hg17439135
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516880
Supporting Variants
Samples
Known GenesSPANXA1, SPANXA2, SPANXA2-OT1, SPANXC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672692
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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