A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6620009



Internal ID20993080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36915814..36924819hg38UCSC Ensembl
chr7:36955419..36964424hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg389006
hg199006
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156200
Samples
Known GenesELMO1, MIR1200
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6620009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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