A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603983



Internal ID20977054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:72918981..72920551hg38UCSC Ensembl
chr7:72389518..72391088hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg381571
hg191571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159429
Samples
Known GenesPOM121
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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