A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610199



Internal ID20983270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100694401..100976100hg38UCSC Ensembl
chr7:100292024..100619381hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38281700
hg19327358
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227583
Samples
Known GenesACHE, EPHB4, EPO, MIR6875, MUC12, POP7, SLC12A9, SRRT, TRIP6, UFSP1, ZAN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610199
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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