A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604276



Internal ID20977347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78276471..78689075hg38UCSC Ensembl
chr7:77905788..78318391hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg38412605
hg19412604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158906
Samples
Known GenesMAGI2, MIR548AU, RPL13AP17
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604276
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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