A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615941



Internal ID20989012
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:91995104..91995547hg38UCSC Ensembl
chr7:91624418..91624861hg19UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg38444
hg19444
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18159952
Samples
Known GenesAKAP9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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