A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997966



Internal ID16944232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46614417..46615216hg38UCSC Ensembl
Outerchr10:46934401..46935200hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951575
Supporting Variants
SamplesBILGI_BIOE
Known GenesFAM35BP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997966
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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