A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951832



Internal ID17300706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:147949669..148015370hg38UCSC Ensembl
Outerchr1:147421901..147487600hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3865702
hg1965700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997273
SamplesBILGI_BIOE
Known GenesGPR89B, GPR89C, PDZK1P1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951832
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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