A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603437



Internal ID20976508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111082638..111482101hg38UCSC Ensembl
chr7:110722694..111122157hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38399464
hg19399464
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18148506
Samples
Known GenesIMMP2L, LRRN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603437
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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