A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436177



Internal ID21093730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:112156677..112158094hg38UCSC Ensembl
chr9:114918957..114920374hg19UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg381418
hg191418
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18175241
Samples
Known GenesMIR3134, SUSD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436177
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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