A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604823



Internal ID20977894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111183698..111418814hg38UCSC Ensembl
chr7:110823754..111058870hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38235117
hg19235117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7052n223
Supporting Variantsnssv18149121
Samples
Known GenesIMMP2L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604823
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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