A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601174



Internal ID20974245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:73715532..73716261hg38UCSC Ensembl
chr7:73129862..73130591hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159467
Samples
Known GenesSTX1A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601174
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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