A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698171



Internal ID15088137
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:141608987..141667150hg38UCSC Ensembl
InnerchrX:140697115..140755302hg19UCSC Ensembl
InnerchrX:140524781..140582968hg18UCSC Ensembl
InnerchrX:140422635..140480822hg17UCSC Ensembl
CytobandXq27.2
Allele length
AssemblyAllele length
hg3858164
hg1958188
hg1858188
hg1758188
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516880
Supporting Variants
Samples
Known GenesSPANXA2-OT1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698171
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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