A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607441



Internal ID20980512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:72525501..72847000hg38UCSC Ensembl
chr7:71990486..72317581hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38321500
hg19327096
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159390
Samples
Known GenesMIR4650-1, MIR4650-2, SBDSP1, TYW1B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607441
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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