A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400904



Internal ID21058457
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76613925..76619697hg38UCSC Ensembl
chr5:75909750..75915522hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg385773
hg195773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134490
Samples
Known GenesF2RL2, IQGAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400904
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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