A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997930



Internal ID16944196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:34814373..34815772hg38UCSC Ensembl
Outerchr10:35103301..35104700hg19UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg381400
hg191400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951538
Supporting Variants
SamplesBILGI_BIOE
Known GenesPARD3, PARD3-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997930
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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