A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614093



Internal ID20987164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:88299866..88305394hg38UCSC Ensembl
chr7:87929181..87934709hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg385529
hg195529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161939
Samples
Known GenesSTEAP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614093
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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