A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603843



Internal ID20976914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:736041..764223hg38UCSC Ensembl
chr7:775678..803860hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3828183
hg1928183
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159458
Samples
Known GenesHEATR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603843
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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