A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617600



Internal ID20990671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93189354..93189819hg38UCSC Ensembl
chr7:92818667..92819132hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161752
Samples
Known GenesHEPACAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617600
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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