A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv664666



Internal ID15401318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:48026897..48071612hg38UCSC Ensembl
InnerchrX:47886291..47930979hg19UCSC Ensembl
InnerchrX:47771235..47815923hg18UCSC Ensembl
InnerchrX:47642545..47687233hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3844716
hg1944689
hg1844689
hg1744689
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517350
Supporting Variants
Samples
Known GenesZNF630
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv664666
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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