A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997955



Internal ID16944221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:43055053..43105452hg38UCSC Ensembl
Outerchr10:43550501..43600900hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3850400
hg1950400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951564
Supporting Variants
SamplesBILGI_BIOE
Known GenesRET
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997955
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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