A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611613



Internal ID20984684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74114737..74115280hg38UCSC Ensembl
chr7:73529067..73529610hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38544
hg19544
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159504
Samples
Known GenesLIMK1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611613
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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