A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614998



Internal ID20988069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:92458112..92459112hg38UCSC Ensembl
chr7:92087426..92088426hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg381001
hg191001
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159987
Samples
Known GenesGATAD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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