A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950296



Internal ID17299170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:195065372..195088171hg38UCSC Ensembl
Outerchr3:194786101..194808900hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3822800
hg1922800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996588
SamplesBILGI_BIOE
Known GenesXXYLT1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950296
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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