A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604557



Internal ID20977628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104417753..104419984hg38UCSC Ensembl
chr7:104058201..104060432hg19UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg382232
hg192232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151979
Samples
Known GenesLHFPL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604557
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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