A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701338



Internal ID15091304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141254378..141463161hg38UCSC Ensembl
InnerchrX:140348507..140551155hg19UCSC Ensembl
InnerchrX:140176173..140378821hg18UCSC Ensembl
InnerchrX:140074027..140276675hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg38208784
hg19202649
hg18202649
hg17202649
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516880
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701338
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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