A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18192501



Internal ID20759542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:74211424..74219052hg38UCSC Ensembl
chr9:76826340..76833968hg19UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg387629
hg197629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6452329
Supporting Variants
Samples
Known GenesMIR6130
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18192501
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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