A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617648



Internal ID20990719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:93199689..93200253hg38UCSC Ensembl
chr7:92829002..92829566hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg38565
hg19565
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161754
Samples
Known GenesHEPACAM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617648
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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