A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952151



Internal ID16954338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:56106132..56108731hg38UCSC Ensembl
Outerchr19:56617501..56620100hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999893
SamplesBILGI_BIOE
Known GenesZNF787
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952151
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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