A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395830



Internal ID21053383
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:73238257..73244803hg38UCSC Ensembl
chr6:73947980..73954526hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg386547
hg196547
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147477
Samples
Known GenesKHDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395830
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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