A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608866



Internal ID20981937
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93315101..93316000hg38UCSC Ensembl
chr7:92944413..92945312hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161767
Samples
Known GenesCCDC132
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608866
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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