A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950621



Internal ID17299495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:37031600..37038499hg38UCSC Ensembl
Outerchr1:37497201..37504100hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg386900
hg196900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997125
SamplesBILGI_BIOE
Known GenesGRIK3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950621
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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