A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6436609



Internal ID21094162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:104759898..104765468hg38UCSC Ensembl
chr9:107522179..107527749hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg385571
hg195571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18173308
Samples
Known GenesNIPSNAP3A, NIPSNAP3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6436609
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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