A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6443749



Internal ID21101302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127832865..127834779hg38UCSC Ensembl
chr9:130595144..130597058hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg381915
hg191915
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18176828
Samples
Known GenesENG
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6443749
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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