A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6603968



Internal ID20977039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:35873199..35873744hg38UCSC Ensembl
chr7:35912809..35913354hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38546
hg19546
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18153709
Samples
Known GenesSEPT7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6603968
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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