A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv665531



Internal ID15402183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52766862..52767002hg38UCSC Ensembl
Innerchr10:54526622..54526762hg19UCSC Ensembl
Innerchr10:54196628..54196768hg18UCSC Ensembl
Innerchr10:54196628..54196768hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38141
hg19141
hg18141
hg17141
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515970
Supporting Variants
Samples
Known GenesMBL2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv665531
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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