A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694219



Internal ID15084185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141340425..141344617hg38UCSC Ensembl
InnerchrX:140434569..140438761hg19UCSC Ensembl
InnerchrX:140262235..140266427hg18UCSC Ensembl
InnerchrX:140160089..140164281hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg384193
hg194193
hg184193
hg174193
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516880
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694219
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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