A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601451



Internal ID20974522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75058519..75060679hg38UCSC Ensembl
chr7:74474331..74476492hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg382161
hg192162
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159572
Samples
Known GenesWBSCR16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601451
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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