A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2758744



Internal ID17414928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:13229614..13234697hg38UCSC Ensembl
Innerchr10:13271614..13276697hg19UCSC Ensembl
Innerchr10:13311620..13316703hg18UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385084
hg195084
hg185084
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv971902
Supporting Variants
SamplesHGDP00542
Known GenesUCMA
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2758744
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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