A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6557753



Internal ID20930824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:40612861..40613751hg38UCSC Ensembl
chr7:40652460..40653350hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38891
hg19891
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18275311
Samples
Known GenesC7orf10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6557753
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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