A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702675



Internal ID15092641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141136956..141254378hg38UCSC Ensembl
InnerchrX:140231141..140348507hg19UCSC Ensembl
InnerchrX:140058807..140176173hg18UCSC Ensembl
InnerchrX:139956661..140074027hg17UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38117423
hg19117367
hg18117367
hg17117367
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516880
Supporting Variants
Samples
Known GenesLDOC1, SPANXC
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702675
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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