A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997967



Internal ID16944233
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46399463..46609616hg38UCSC Ensembl
Outerchr10:46940001..47150300hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg38210154
hg19210300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951576
Supporting Variants
SamplesBILGI_BIOE
Known GenesGPRIN2, HNRNPA1P33, LINC00842, LOC100996758, NPY4R, SYT15
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997967
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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