A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619474



Internal ID20992545
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:23310223..23319034hg38UCSC Ensembl
chr7:23349842..23358653hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg388812
hg198812
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154912
Samples
Known GenesIGF2BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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