A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701438



Internal ID15438090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr18:7732919..7760500hg38UCSC Ensembl
Innerchr18:7732917..7760498hg19UCSC Ensembl
Innerchr18:7722917..7750498hg18UCSC Ensembl
Innerchr18:7722917..7750498hg17UCSC Ensembl
Cytoband18p11.23
Allele length
AssemblyAllele length
hg3827582
hg1927582
hg1827582
hg1727582
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525328
Supporting Variants
Samples
Known GenesPTPRM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701438
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer