A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998064



Internal ID17291016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122582185..122595384hg38UCSC Ensembl
Outerchr10:124341701..124354900hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3813200
hg1913200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951865
Supporting Variants
SamplesBILGI_BIOE
Known GenesDMBT1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998064
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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