A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3574995



Internal ID18526590
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:50971269..50994022hg38UCSC Ensembl
Innerchr19:51474525..51497278hg19UCSC Ensembl
Innerchr19:56166337..56189090hg18UCSC Ensembl
Cytoband19q13.33
Allele length
AssemblyAllele length
hg3822754
hg1922754
hg1822754
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064207
Supporting Variants
Samples
Known GenesKLK7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3574995
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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