A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614078



Internal ID20987149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108688733..108959842hg38UCSC Ensembl
chr7:108329177..108599899hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38271110
hg19270723
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147042
Samples
Known GenesC7orf66
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614078
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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