A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701083



Internal ID15437735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:6236589..6307568hg38UCSC Ensembl
InnerchrX:6154630..6225609hg19UCSC Ensembl
InnerchrX:6164630..6235609hg18UCSC Ensembl
InnerchrX:6014366..6085345hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3870980
hg1970980
hg1870980
hg1770980
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525039
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701083
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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