A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697357



Internal ID15087323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:150629881..150636791hg38UCSC Ensembl
InnerchrX:149798354..149805264hg19UCSC Ensembl
InnerchrX:149549012..149555922hg18UCSC Ensembl
InnerchrX:149468922..149475832hg17UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg386911
hg196911
hg186911
hg176911
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520338
Supporting Variants
Samples
Known GenesMTM1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697357
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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