A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600806



Internal ID20973877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:30369630..30370200hg38UCSC Ensembl
chr7:30409246..30409816hg19UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38571
hg19571
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155696
Samples
Known GenesDKFZP586I1420
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600806
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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