A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611172



Internal ID20984243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78554818..78574288hg38UCSC Ensembl
chr7:78184135..78203605hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3819471
hg1919471
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18158932
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611172
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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