A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170231



Internal ID21314292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:18598054..18677625hg38UCSC Ensembl
Outerchr7:18593689..18680512hg38UCSC Ensembl
Innerchr7:18637677..18717248hg19UCSC Ensembl
Outerchr7:18633312..18720135hg19UCSC Ensembl
Innerchr7:18604202..18683773hg18UCSC Ensembl
Outerchr7:18599837..18686660hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3886824
hg1986824
hg1886824
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14241134
SamplesNGO_32
Known GenesHDAC9
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170231
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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