A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694979



Internal ID15084945
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:135374609..135533826hg38UCSC Ensembl
InnerchrX:134508534..134667751hg19UCSC Ensembl
InnerchrX:134336200..134495417hg18UCSC Ensembl
InnerchrX:134234054..134393271hg17UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg38159218
hg19159218
hg18159218
hg17159218
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522205
Supporting Variants
Samples
Known GenesDDX26B, LINC00086, LOC100506790
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694979
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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