A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv689191



Internal ID15425843
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:128680560..128690018hg38UCSC Ensembl
InnerchrX:127814538..127823996hg19UCSC Ensembl
InnerchrX:127642219..127651677hg18UCSC Ensembl
InnerchrX:127540073..127549531hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg389459
hg199459
hg189459
hg179459
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517752
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv689191
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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