A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3170153



Internal ID21314214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:37700299..37772775hg38UCSC Ensembl
Outerchr7:37691941..37776229hg38UCSC Ensembl
Innerchr7:37739901..37812377hg19UCSC Ensembl
Outerchr7:37731543..37815831hg19UCSC Ensembl
Innerchr7:37706426..37778902hg18UCSC Ensembl
Outerchr7:37698068..37782356hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3884289
hg1984289
hg1884289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14242800
SamplesMLY_15
Known GenesGPR141
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3170153
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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