A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv670021



Internal ID15059987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:24115349..24173404hg38UCSC Ensembl
InnerchrX:24133466..24191521hg19UCSC Ensembl
InnerchrX:24043387..24101442hg18UCSC Ensembl
InnerchrX:23893123..23951178hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3858056
hg1958056
hg1858056
hg1758056
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516667
Supporting Variants
Samples
Known GenesZFX, ZFX-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv670021
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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