A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617397



Internal ID20990468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111266147..111599820hg38UCSC Ensembl
chr7:110906203..111239876hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38333674
hg19333674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7056n223
Supporting Variantsnssv18149152
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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