A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952155



Internal ID17301029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:58452234..58457833hg38UCSC Ensembl
Outerchr19:58963601..58969200hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999897
SamplesBILGI_BIOE
Known GenesZNF324B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952155
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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