A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692236



Internal ID15082202
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:24115349..24168904hg38UCSC Ensembl
InnerchrX:24133466..24187021hg19UCSC Ensembl
InnerchrX:24043387..24096942hg18UCSC Ensembl
InnerchrX:23893123..23946678hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3853556
hg1953556
hg1853556
hg1753556
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)nssv692236
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer