A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516667



Internal ID15097274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:24115349..24190892hg38UCSC Ensembl
InnerchrX:24133466..24209009hg19UCSC Ensembl
InnerchrX:24043387..24118930hg18UCSC Ensembl
InnerchrX:23893123..23968666hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3875544
hg1975544
hg1875544
hg1775544
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv504n21
Supporting Variantsnssv688355, nssv692236, nssv678443, nssv670021, nssv659290, nssv679242
Samples
Known GenesZFX, ZFX-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516667
Frequency
Sample Size2026
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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