A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700259



Internal ID15436911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:51454859..51498820hg38UCSC Ensembl
InnerchrX:51197711..51241672hg19UCSC Ensembl
InnerchrX:51214451..51258412hg18UCSC Ensembl
InnerchrX:51030747..51074708hg17UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3843962
hg1943962
hg1843962
hg1743962
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524351
Supporting Variants
Samples
Known GenesNUDT11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700259
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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