A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997788



Internal ID19157325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:71457056..71496462hg38UCSC Ensembl
Innerchr4:72322773..72362179hg19UCSC Ensembl
Innerchr4:72541637..72581043hg18UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3839407
hg1939407
hg1839407
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3633077
Samples
Known GenesSLC4A4
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997788
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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