A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606628



Internal ID20979699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23410001..23411800hg38UCSC Ensembl
chr7:23449620..23451419hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154919
Samples
Known GenesIGF2BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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