A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv977704



Internal ID18266224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:41831415..41832826hg38UCSC Ensembl
Innerchr15:42123613..42125024hg19UCSC Ensembl
Innerchr15:39910905..39912316hg18UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg381412
hg191412
hg181412
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2020179, nssv2020184, nssv2020182, nssv2020186, nssv2020187, nssv2020180, nssv2020181, nssv2020183, nssv2020185, nssv2020178
SamplesHGDP01284, HGDP00665, HGDP00998, HGDP00521, HGDP00778, HGDP01307, HGDP00542, HGDP01029, HGDP00456, HGDP00927
Known GenesJMJD7, JMJD7-PLA2G4B
MethodSequencing
Analysislineage specific fixed duplications
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nsv977704
Frequency
Sample Size10
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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