A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398741



Internal ID21056294
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:27314958..28461291hg38UCSC Ensembl
chr6:27282737..28429068hg19UCSC Ensembl
Cytoband6p22.1
Allele length
AssemblyAllele length
hg381146334
hg191146332
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18218779
Samples
Known GenesHIST1H1B, HIST1H2AI, HIST1H2AJ, HIST1H2AK, HIST1H2AL, HIST1H2AM, HIST1H2BL, HIST1H2BM, HIST1H2BN, HIST1H2BO, HIST1H3H, HIST1H3I, HIST1H3J, HIST1H4J, HIST1H4K, HIST1H4L, LINC01012, LOC100131289, NKAPL, OR2B2, OR2B6, PGBD1, TOB2P1, VN1R10P, ZKSCAN3, ZKSCAN4, ZKSCAN8, ZNF165, ZNF184, ZNF192P1, ZNF204P, ZNF391, ZSCAN12, ZSCAN12P1, ZSCAN16, ZSCAN16-AS1, ZSCAN23, ZSCAN26, ZSCAN31, ZSCAN9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398741
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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