A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697934



Internal ID15434586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:68154824..68162978hg38UCSC Ensembl
Innerchr10:69914581..69922735hg19UCSC Ensembl
Innerchr10:69584587..69592741hg18UCSC Ensembl
Innerchr10:69584587..69592741hg17UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg388155
hg198155
hg188155
hg178155
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521328
Supporting Variants
Samples
Known GenesMYPN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697934
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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