A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695971



Internal ID15432623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:22299406..22299596hg38UCSC Ensembl
InnerchrX:22317523..22317713hg19UCSC Ensembl
InnerchrX:22227444..22227634hg18UCSC Ensembl
InnerchrX:22077180..22077370hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38191
hg19191
hg18191
hg17191
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518528
Supporting Variants
Samples
Known GenesLOC100873065
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695971
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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