A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523984



Internal ID15104591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:109674544..109723196hg38UCSC Ensembl
InnerchrX:108917773..108966425hg19UCSC Ensembl
InnerchrX:108804429..108853081hg18UCSC Ensembl
InnerchrX:108723918..108772570hg17UCSC Ensembl
CytobandXq22.3
Allele length
AssemblyAllele length
hg3848653
hg1948653
hg1848653
hg1748653
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv699840
Samples
Known GenesACSL4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523984
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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