A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608681



Internal ID20981752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111031381..111304671hg38UCSC Ensembl
chr7:110671437..110944727hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38273291
hg19273291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148503
Samples
Known GenesIMMP2L, LRRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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