A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604626



Internal ID20977697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:109897304..110005979hg38UCSC Ensembl
chr7:109537361..109646036hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38108676
hg19108676
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147829
Samples
Known GenesEIF3IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604626
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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