A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680829



Internal ID15070795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155545046..155699751hg38UCSC Ensembl
InnerchrX:154774707..154929412hg19UCSC Ensembl
InnerchrX:154427901..154582606hg18UCSC Ensembl
InnerchrX:154338411..154493116hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38154706
hg19154706
hg18154706
hg17154706
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520699
Supporting Variants
Samples
Known GenesTMLHE
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680829
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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