A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702657



Internal ID15439309
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:118562662..118630652hg38UCSC Ensembl
InnerchrX:117696625..117764615hg19UCSC Ensembl
InnerchrX:117580653..117648643hg18UCSC Ensembl
InnerchrX:117478507..117546497hg17UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg3867991
hg1967991
hg1867991
hg1767991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517257
Supporting Variants
Samples
Known GenesDOCK11
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702657
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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