A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697641



Internal ID15434293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:150454390..150455827hg38UCSC Ensembl
InnerchrX:149622656..149624093hg19UCSC Ensembl
InnerchrX:149373314..149374751hg18UCSC Ensembl
InnerchrX:149293224..149294661hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381438
hg191438
hg181438
hg171438
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520835
Supporting Variants
Samples
Known GenesMAMLD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697641
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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