A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv654979



Internal ID15391631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:128683498..128799692hg38UCSC Ensembl
InnerchrX:127817476..127933670hg19UCSC Ensembl
InnerchrX:127645157..127761351hg18UCSC Ensembl
InnerchrX:127543011..127659205hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38116195
hg19116195
hg18116195
hg17116195
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)nssv654979
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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