A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600816



Internal ID20973887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:29625601..29650200hg38UCSC Ensembl
chr7:29665217..29689816hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3824600
hg1924600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155654
Samples
Known GenesLOC646762
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600816
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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