A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527358



Internal ID15107965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:135908919..135964659hg38UCSC Ensembl
InnerchrX:134991078..135046818hg19UCSC Ensembl
InnerchrX:134818744..134874484hg18UCSC Ensembl
InnerchrX:134716598..134772338hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3855741
hg1955741
hg1855741
hg1755741
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703788
Samples
Known GenesMMGT1, SAGE1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527358
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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