A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6612976



Internal ID20986047
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:26816959..26817525hg38UCSC Ensembl
chr7:26856578..26857144hg19UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg38567
hg19567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18155616
Samples
Known GenesSKAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6612976
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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