A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614891



Internal ID20987962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:110845639..110881247hg38UCSC Ensembl
chr7:110485695..110521303hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3835609
hg1935609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148465
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614891
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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