A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv950896



Internal ID16953083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:92803119..92809918hg38UCSC Ensembl
Outerchr9:95565401..95572200hg19UCSC Ensembl
Cytoband9q22.31
Allele length
AssemblyAllele length
hg386800
hg196800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996929
SamplesBILGI_BIOE
Known GenesANKRD19P
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv950896
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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