A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17993635



Internal ID20560675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7513775..7515611hg38UCSC Ensembl
chr11:7535006..7536842hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg381837
hg191837
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6440642
Supporting Variants
Samples
Known GenesPPFIBP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17993635
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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